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Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score
Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of p...
| Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231039/ https://www.ncbi.nlm.nih.gov/pubmed/30456254 http://dx.doi.org/10.1016/j.dib.2018.10.125 |
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| author | Moulin, Philippe Dufour, Robert Averna, Maurizio Arca, Marcello Cefalù, Angelo B. Noto, Davide D’Erasmo, Laura Di Costanzo, Alessia Marçais, Christophe Walther, Luis Antonio Alvarez-Sala Banach, Maciej Borén, Jan Cramb, Robert Gouni-Berthold, Ioanna Hughes, Elizabeth Johnson, Colin Pintó, Xavier Reiner, Željko van Lennep, Jeanine Roeters Soran, Handrean Stefanutti, Claudia Stroes, Erik Bruckert, Eric |
| author_facet | Moulin, Philippe Dufour, Robert Averna, Maurizio Arca, Marcello Cefalù, Angelo B. Noto, Davide D’Erasmo, Laura Di Costanzo, Alessia Marçais, Christophe Walther, Luis Antonio Alvarez-Sala Banach, Maciej Borén, Jan Cramb, Robert Gouni-Berthold, Ioanna Hughes, Elizabeth Johnson, Colin Pintó, Xavier Reiner, Željko van Lennep, Jeanine Roeters Soran, Handrean Stefanutti, Claudia Stroes, Erik Bruckert, Eric |
| author_sort | Moulin, Philippe |
| collection | PubMed |
| description | Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS), from the validation and replication cohorts. |
| format | Online Article Text |
| id | pubmed-6231039 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2018 |
| publisher | Elsevier |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-62310392018-11-19 Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score Moulin, Philippe Dufour, Robert Averna, Maurizio Arca, Marcello Cefalù, Angelo B. Noto, Davide D’Erasmo, Laura Di Costanzo, Alessia Marçais, Christophe Walther, Luis Antonio Alvarez-Sala Banach, Maciej Borén, Jan Cramb, Robert Gouni-Berthold, Ioanna Hughes, Elizabeth Johnson, Colin Pintó, Xavier Reiner, Željko van Lennep, Jeanine Roeters Soran, Handrean Stefanutti, Claudia Stroes, Erik Bruckert, Eric Data Brief Genetics, Genomics and Molecular Biology Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS), from the validation and replication cohorts. Elsevier 2018-10-27 /pmc/articles/PMC6231039/ /pubmed/30456254 http://dx.doi.org/10.1016/j.dib.2018.10.125 Text en © 2018 Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
| spellingShingle | Genetics, Genomics and Molecular Biology Moulin, Philippe Dufour, Robert Averna, Maurizio Arca, Marcello Cefalù, Angelo B. Noto, Davide D’Erasmo, Laura Di Costanzo, Alessia Marçais, Christophe Walther, Luis Antonio Alvarez-Sala Banach, Maciej Borén, Jan Cramb, Robert Gouni-Berthold, Ioanna Hughes, Elizabeth Johnson, Colin Pintó, Xavier Reiner, Željko van Lennep, Jeanine Roeters Soran, Handrean Stefanutti, Claudia Stroes, Erik Bruckert, Eric Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score |
| title | Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score |
| title_full | Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score |
| title_fullStr | Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score |
| title_full_unstemmed | Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score |
| title_short | Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score |
| title_sort | characterisation of patients with familial chylomicronaemia syndrome (fcs) and multifactorial chylomicronaemia syndrome (mcs): establishment of an fcs clinical diagnostic score |
| topic | Genetics, Genomics and Molecular Biology |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231039/ https://www.ncbi.nlm.nih.gov/pubmed/30456254 http://dx.doi.org/10.1016/j.dib.2018.10.125 |
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