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“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747945/ https://www.ncbi.nlm.nih.gov/pubmed/29287597 http://dx.doi.org/10.1186/s12969-017-0215-8 |
| _version_ | 1783289338094682112 |
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| author | Arowolo, Afolake T. Adeola, Henry A. Khumalo, Nonhlanhla P. |
| author_facet | Arowolo, Afolake T. Adeola, Henry A. Khumalo, Nonhlanhla P. |
| author_sort | Arowolo, Afolake T. |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-5747945 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2017 |
| publisher | BioMed Central |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-57479452018-01-03 “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” Arowolo, Afolake T. Adeola, Henry A. Khumalo, Nonhlanhla P. Pediatr Rheumatol Online J Letter to the Editor BioMed Central 2017-12-29 /pmc/articles/PMC5747945/ /pubmed/29287597 http://dx.doi.org/10.1186/s12969-017-0215-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
| spellingShingle | Letter to the Editor Arowolo, Afolake T. Adeola, Henry A. Khumalo, Nonhlanhla P. “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” |
| title | “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” |
| title_full | “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” |
| title_fullStr | “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” |
| title_full_unstemmed | “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” |
| title_short | “Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease” |
| title_sort | “next generation sequencing identifies mutations in gnptg gene as a cause of familial form of scleroderma-like disease” |
| topic | Letter to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747945/ https://www.ncbi.nlm.nih.gov/pubmed/29287597 http://dx.doi.org/10.1186/s12969-017-0215-8 |
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