Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain-Reference-Cited by-同舟云学术

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain

Published:2015-12 Issue:6 Volume:97 Page:878-885
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Logan Clare V.,Cossins Judith,Rodríguez Cruz Pedro M.,Parry David A.,Maxwell Susan,Martínez-Martínez Pilar,Riepsaame Joey,Abdelhamed Zakia A.,Lake Alice V.R.,Moran Maria,Robb Stephanie,Chow Gabriel,Sewry Caroline,Hopkins Philip M.,Sheridan Eamonn,Jayawant Sandeep,Palace Jacqueline,Johnson Colin A.,Beeson David

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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