Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: urinary organic acid profiles and expanded spectrum of mutations.
about
Multi-dimensional Roles of Ketone Bodies in Fuel Metabolism, Signaling, and Therapeutics.Mitochondrial 3-Hydroxy-3-Methylglutaryl-CoA Synthase Deficiency: Unique Presenting Laboratory Values and a Review of Biochemical and Clinical Features.Human Mitochondrial HMG-CoA Synthase Deficiency: Role of Enzyme Dimerization Surface and Characterization of Three New Patients.
P2860
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: urinary organic acid profiles and expanded spectrum of mutations.
description
2014 nî lūn-bûn
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2014年学术文章
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2014年学术文章
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2014年学术文章
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name
Mitochondrial 3-hydroxy-3-meth ...... xpanded spectrum of mutations.
@en
type
label
Mitochondrial 3-hydroxy-3-meth ...... xpanded spectrum of mutations.
@en
prefLabel
Mitochondrial 3-hydroxy-3-meth ...... xpanded spectrum of mutations.
@en
P2093
P2860
P1476
Mitochondrial 3-hydroxy-3-meth ...... xpanded spectrum of mutations.
@en
P2093
Avihu Boneh
David Johnson
Heidi Peters
James J Pitt
Johannes Zschocke
Joy Yaplito-Lee
Katrin Hinderhofer
Stefanie Wieser
P2860
P2888
P304
P356
10.1007/S10545-014-9801-9
P577
2014-12-16T00:00:00Z
P6179
1016533708