Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome

Detalles Bibliográficos
Autores principales: Oh, Seung Joon, Kim, Song-Ee, Lee, Sang Eun, Kim, Soo-Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2016
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969485/
https://www.ncbi.nlm.nih.gov/pubmed/27489438
http://dx.doi.org/10.5021/ad.2016.28.4.503
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author Oh, Seung Joon
Kim, Song-Ee
Lee, Sang Eun
Kim, Soo-Chan
author_facet Oh, Seung Joon
Kim, Song-Ee
Lee, Sang Eun
Kim, Soo-Chan
author_sort Oh, Seung Joon
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spelling pubmed-49694852016-08-03 Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome Oh, Seung Joon Kim, Song-Ee Lee, Sang Eun Kim, Soo-Chan Ann Dermatol Brief Report Korean Dermatological Association; The Korean Society for Investigative Dermatology 2016-08 2016-07-26 /pmc/articles/PMC4969485/ /pubmed/27489438 http://dx.doi.org/10.5021/ad.2016.28.4.503 Text en Copyright © 2016 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Oh, Seung Joon
Kim, Song-Ee
Lee, Sang Eun
Kim, Soo-Chan
Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
title Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
title_full Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
title_fullStr Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
title_full_unstemmed Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
title_short Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
title_sort homozygous deletion mutation of the fermt1 gene in a chinese patient with kindler syndrome
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969485/
https://www.ncbi.nlm.nih.gov/pubmed/27489438
http://dx.doi.org/10.5021/ad.2016.28.4.503
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