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Congenital disorder of glycosylation type Ia in a 6-year-old girl with a mild intellectual phenotype: Two novel PMM2 mutations

✍ Scribed by D. Coman; S. Klingberg; D. Morris; J. McGill; H. Mercer


Publisher
Springer
Year
2005
Tongue
English
Weight
76 KB
Volume
28
Category
Article
ISSN
0141-8955

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