Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms.
about
Revealing the Protein Propionylation Activity of the Histone Acetyltransferase Males absent on the first (MOF).Clinical and genetic characteristics of patients with fatty acid oxidation disorders identified by newborn screening.An unusually high frequency of SCAD deficiency caused by two pathogenic variants in the ACADS gene and its relationship to the ethnic structure in Slovakia.
P2860
Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms.
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
@zh-my
2017年学术文章
@zh-sg
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
Short-chain acyl-CoA dehydroge ...... d possible disease mechanisms.
@en
Short-chain acyl-CoA dehydroge ...... d possible disease mechanisms.
@nl
type
label
Short-chain acyl-CoA dehydroge ...... d possible disease mechanisms.
@en
Short-chain acyl-CoA dehydroge ...... d possible disease mechanisms.
@nl
prefLabel
Short-chain acyl-CoA dehydroge ...... d possible disease mechanisms.
@en
Short-chain acyl-CoA dehydroge ...... d possible disease mechanisms.
@nl
P2860
P1476
Short-chain acyl-CoA dehydroge ...... d possible disease mechanisms.
@en
P2093
Niels Gregersen
P2860
P2888
P304
P356
10.1007/S10545-017-0047-1
P577
2017-05-17T00:00:00Z