Functional studies of tyrosine hydroxylase missense variants reveal distinct patterns of molecular defects in Dopa-responsive dystonia.
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Personalized biochemistry and biophysics.A new knock-in mouse model of l-DOPA-responsive dystonia.A commentary on the utility of a new L-DOPA-responsive dystonia mouse modelTyrosine and tryptophan hydroxylases as therapeutic targets in human disease.Parkinsonism without dopamine neuron degeneration in aged l-dopa-responsive dystonia knockin mice.Dopa-Responsive Dystonia in Han Chinese Patients: One Novel Heterozygous Mutation in GTP Cyclohydrolase 1 (GCH1) and Three Known Mutations in TH.Brain catecholamine depletion and motor impairment in a Th knock-in mouse with type B tyrosine hydroxylase deficiency.
P2860
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P2860
Functional studies of tyrosine hydroxylase missense variants reveal distinct patterns of molecular defects in Dopa-responsive dystonia.
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
@wuu
2014年论文
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2014年论文
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name
Functional studies of tyrosine ...... s in Dopa-responsive dystonia.
@en
Functional studies of tyrosine ...... s in Dopa-responsive dystonia.
@nl
type
label
Functional studies of tyrosine ...... s in Dopa-responsive dystonia.
@en
Functional studies of tyrosine ...... s in Dopa-responsive dystonia.
@nl
prefLabel
Functional studies of tyrosine ...... s in Dopa-responsive dystonia.
@en
Functional studies of tyrosine ...... s in Dopa-responsive dystonia.
@nl
P2093
P2860
P356
P1433
P1476
Functional studies of tyrosine ...... s in Dopa-responsive dystonia.
@en
P2093
Agnete Fossbakk
Per M Knappskog
Rune Kleppe
P2860
P304
P356
10.1002/HUMU.22565
P577
2014-06-03T00:00:00Z