Mutations in PMM2 that cause congenital disorders of...

Human Mutation 2000 Vol. 16; Iss. 5

Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)

G. Matthijs, E. Schollen, C. Bjursell, A. Erlandson, H. Freeze, F. Imtiaz, S. Kjaergaard, T. Martinsson, M. Schwartz, N. Seta, S. Vuillaumier-Barrot, V. Westphal, B. Winchester
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Volume:
16
Year:
2000
Language:
english
Pages:
9
DOI:
10.1002/1098-1004(200011)16:53.0.co;2-y
File:
PDF, 345 KB
english, 2000
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