Novel mutation causing partial biotinidase deficiency in a Syrian boy with infantile spasms and retardation
about
Infantile spasms: review of the literature and personal experience.Profound biotinidase deficiency in a child with predominantly spinal cord disease.Screening of Inherited Metabolic Disorders in Infants with Infantile Spasms.Metabolic etiologies in West syndrome.The genetic landscape of infantile spasms
P2860
Novel mutation causing partial biotinidase deficiency in a Syrian boy with infantile spasms and retardation
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
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2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
name
Novel mutation causing partial ...... fantile spasms and retardation
@ast
Novel mutation causing partial ...... fantile spasms and retardation
@en
Novel mutation causing partial ...... fantile spasms and retardation
@nl
type
label
Novel mutation causing partial ...... fantile spasms and retardation
@ast
Novel mutation causing partial ...... fantile spasms and retardation
@en
Novel mutation causing partial ...... fantile spasms and retardation
@nl
prefLabel
Novel mutation causing partial ...... fantile spasms and retardation
@ast
Novel mutation causing partial ...... fantile spasms and retardation
@en
Novel mutation causing partial ...... fantile spasms and retardation
@nl
P2860
P50
P1476
Novel mutation causing partial ...... fantile spasms and retardation
@en
P2093
Amal C Rahi
Pascale Karam
P2860
P304
P356
10.1177/08830738060210110301
P407
P577
2006-11-01T00:00:00Z