Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome

PURPOSE: Weill-Marchesani syndrome (WMS) is a rare connective tissue disorder, characterized by short stature, microspherophakic lens, and stubby hands and feet (brachydactyly). WMS is caused by mutations in the FBN1, ADAMTS10, and LTBP2 genes. Mutations in the LTBP2 and ADAMTS17 genes cause a WMS-l...

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Detalles Bibliográficos
Autores principales: Shah, Mohd Hussain, Bhat, Vishwanath, Shetty, Jyoti S., Kumar, Arun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057248/
https://www.ncbi.nlm.nih.gov/pubmed/24940034

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057248/
https://www.ncbi.nlm.nih.gov/pubmed/24940034

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