Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih. (Q51865271)

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scientific article published on 24 June 2009
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Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih.
scientific article published on 24 June 2009

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    Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih. (English)

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