Inherited disorders of gamma-aminobutyric acid metabolism and advances in ALDH5A1 mutation identification.
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Transcriptome-wide Investigation of mRNA/circRNA in miR-184 and Its r.57c > u Mutant Type Treatment of Human Lens Epithelial Cells.Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolismTherapeutic relevance of mTOR inhibition in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.mTOR inhibitors rescue premature lethality and attenuate dysregulation of GABAergic/glutamatergic transcription in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.
P2860
Inherited disorders of gamma-aminobutyric acid metabolism and advances in ALDH5A1 mutation identification.
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
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2014年论文
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2014年论文
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name
Inherited disorders of gamma-a ...... DH5A1 mutation identification.
@ast
Inherited disorders of gamma-a ...... DH5A1 mutation identification.
@en
type
label
Inherited disorders of gamma-a ...... DH5A1 mutation identification.
@ast
Inherited disorders of gamma-a ...... DH5A1 mutation identification.
@en
prefLabel
Inherited disorders of gamma-a ...... DH5A1 mutation identification.
@ast
Inherited disorders of gamma-a ...... DH5A1 mutation identification.
@en
P2093
P2860
P50
P356
P1476
Inherited disorders of gamma-a ...... LDH5A1 mutation identification
@en
P2093
K Michael Gibson
Kara Vogel
William H Theodore
P2860
P304
P356
10.1111/DMCN.12668
P577
2014-12-29T00:00:00Z