Congenital Disorder of Glycosylation Type Ia: Searching for the Origin of Common Mutations in Pmm2

AuthID
 P-004-A68
5
Author(s)
Tipo de Documento
Article
Year published
2007
Publicado
in ANNALS OF HUMAN GENETICS, ISSN: 0003-4800
Volume: 71, Número: 3, Páginas: 348-353 (6)
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Publication Identifiers
Pubmed: 17166182
SCOPUS: 2-s2.0-34247107598
Wos: WOS:000245691800008
Source Identifiers
ISSN: 0003-4800
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