A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case series

Bibliographic Details
Published in:Canadian Medical Association Journal
Main Authors: Rousseau-Nepton, Isabelle, Okubo, Minoru, Grabs, Rosemarie, Mitchell, John, Polychronakos, Constantin, Rodd, Celia
Format: Text
Language:English
Published: Canadian Medical Association 2015
Subjects:
Research
inuit
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312169
http://www.ncbi.nlm.nih.gov/pubmed/25602008
https://doi.org/10.1503/cmaj.140840
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