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A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510937/ https://www.ncbi.nlm.nih.gov/pubmed/31192996 http://dx.doi.org/10.1016/j.jdcr.2019.03.008 |
| _version_ | 1783417499790868480 |
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| author | Kiratli Nalbant, Esra Karaosmanoglu, Nermin Kutlu, Omer Ceylaner, Serdar Eksioglu, Hatice Meral |
| author_facet | Kiratli Nalbant, Esra Karaosmanoglu, Nermin Kutlu, Omer Ceylaner, Serdar Eksioglu, Hatice Meral |
| author_sort | Kiratli Nalbant, Esra |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-6510937 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2019 |
| publisher | Elsevier |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-65109372019-05-20 A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene Kiratli Nalbant, Esra Karaosmanoglu, Nermin Kutlu, Omer Ceylaner, Serdar Eksioglu, Hatice Meral JAAD Case Rep Case Report Elsevier 2019-05-07 /pmc/articles/PMC6510937/ /pubmed/31192996 http://dx.doi.org/10.1016/j.jdcr.2019.03.008 Text en © 2019 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
| spellingShingle | Case Report Kiratli Nalbant, Esra Karaosmanoglu, Nermin Kutlu, Omer Ceylaner, Serdar Eksioglu, Hatice Meral A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene |
| title | A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene |
| title_full | A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene |
| title_fullStr | A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene |
| title_full_unstemmed | A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene |
| title_short | A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene |
| title_sort | rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the pepd gene |
| topic | Case Report |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510937/ https://www.ncbi.nlm.nih.gov/pubmed/31192996 http://dx.doi.org/10.1016/j.jdcr.2019.03.008 |
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