A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case series
Published in: | Canadian Medical Association Journal |
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Main Authors: | , , , , , |
Format: | Text |
Language: | English |
Published: |
Canadian Medical Association
2015
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Subjects: | |
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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