Clinical features and mutations in seven Chinese patients with very long chain acyl-CoA dehydrogenase deficiency.
about
Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the NervesRecurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS databaseA Nonsense Variant in the ACADVL Gene in German Hunting Terrier Dogs with Exercise Induced Metabolic Myopathy.
P2860
Clinical features and mutations in seven Chinese patients with very long chain acyl-CoA dehydrogenase deficiency.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh
2014年學術文章
@zh-hant
name
Clinical features and mutation ...... -CoA dehydrogenase deficiency.
@en
Clinical features and mutation ...... -CoA dehydrogenase deficiency.
@nl
type
label
Clinical features and mutation ...... -CoA dehydrogenase deficiency.
@en
Clinical features and mutation ...... -CoA dehydrogenase deficiency.
@nl
prefLabel
Clinical features and mutation ...... -CoA dehydrogenase deficiency.
@en
Clinical features and mutation ...... -CoA dehydrogenase deficiency.
@nl
P2093
P2860
P1476
Clinical features and mutation ...... -CoA dehydrogenase deficiency.
@en
P2093
Hui-Wen Zhang
Lian-Shu Han
Rui-Nan Zhang
Wen-Juan Qiu
Xue-Fan Gu
P2860
P2888
P304
P356
10.1007/S12519-014-0480-2
P577
2014-05-07T00:00:00Z