Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features.
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Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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2017年學術文章
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name
Mitochondrial 3-Hydroxy-3-Meth ...... hemical and Clinical Features.
@en
Mitochondrial 3-Hydroxy-3-Meth ...... hemical and Clinical Features.
@nl
type
label
Mitochondrial 3-Hydroxy-3-Meth ...... hemical and Clinical Features.
@en
Mitochondrial 3-Hydroxy-3-Meth ...... hemical and Clinical Features.
@nl
prefLabel
Mitochondrial 3-Hydroxy-3-Meth ...... hemical and Clinical Features.
@en
Mitochondrial 3-Hydroxy-3-Meth ...... hemical and Clinical Features.
@nl
P2093
P2860
P356
P1476
Mitochondrial 3-Hydroxy-3-Meth ...... hemical and Clinical Features.
@en
P2093
Brendan Lanpher
David Deyle
Dimitar Gavrilov
Eric W Klee
Erin Conboy
Katherine Agre
Matthew Schultz
Ross Ridsdale
P2860
P356
10.1007/8904_2017_59
P577
2017-10-14T00:00:00Z