Severe speech delay as the presenting symptom of guanidinoacetate methyltransferase deficiency.
about
Inborn errors of creatine metabolism and epilepsy.X-linked creatine transporter deficiency: clinical aspects and pathophysiology.Possible sources and functions of L-homoarginine in the brain: review of the literature and own findings.Feasibility of newborn screening for guanidinoacetate methyltransferase (GAMT) deficiency.
P2860
Severe speech delay as the presenting symptom of guanidinoacetate methyltransferase deficiency.
description
2007 nî lūn-bûn
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2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
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2007年學術文章
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2007年學術文章
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name
Severe speech delay as the pre ...... methyltransferase deficiency.
@en
Severe speech delay as the pre ...... methyltransferase deficiency.
@nl
type
label
Severe speech delay as the pre ...... methyltransferase deficiency.
@en
Severe speech delay as the pre ...... methyltransferase deficiency.
@nl
prefLabel
Severe speech delay as the pre ...... methyltransferase deficiency.
@en
Severe speech delay as the pre ...... methyltransferase deficiency.
@nl
P2093
P2860
P356
P1476
Severe speech delay as the pre ...... methyltransferase deficiency.
@en
P2093
P2860
P304
P356
10.1177/0883073807304015
P577
2007-06-01T00:00:00Z