Identification of a frequent variant in ALG6, the cause of...

Human Mutation 2003 Vol. 22; Iss. 5

Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic

Vibeke Westphal, Ming Xiao, Pui-Yan Kwok, Hudson H. Freeze
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Volume:
22
Year:
2003
Language:
english
Pages:
2
DOI:
10.1002/humu.9195
File:
PDF, 59 KB
english, 2003
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