A founder AGL mutation causing glycogen storage disease...

Canadian Medical Association Journal 2015 / 02 Vol. 187; Iss. 2

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

Rousseau-Nepton, I., Okubo, M., Grabs, R., Mitchell, J., Polychronakos, C., Rodd, C.
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Volume:
187
Language:
english
Journal:
Canadian Medical Association Journal
DOI:
10.1503/cmaj.140840
Date:
February, 2015
File:
PDF, 114 KB
english, 2015
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