Biochemical hallmarks of tyrosine hydroxylase deficiency.

Biochemical hallmarks of tyrosine hydroxylase deficiency.

Item
http://www.wikidata.org/entity/Q42539800
Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiencyAtaxia telangiectasia presenting as dopa-responsive cervical dystonia.Animal models of generalized dystonia.Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental studyEffects of mutations in tyrosine hydroxylase associated with progressive dystonia on the activity and stability of the protein.Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency.Primary dystonia: molecules and mechanisms.The genetics of dystonia: new twists in an old tale.Dopa-Responsive Dystonia in Han Chinese Patients: One Novel Heterozygous Mutation in GTP Cyclohydrolase 1 (GCH1) and Three Known Mutations in TH.Parkinson's Disease Diagnostic Observations (PADDO): study rationale and design of a prospective cohort study for early differentiation of parkinsonism.
P2860

Biochemical hallmarks of tyrosine hydroxylase deficiency.

Item
http://www.wikidata.org/entity/Q42539800
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Biochemical hallmarks of tyrosine hydroxylase deficiency.
@en
Biochemical hallmarks of tyrosine hydroxylase deficiency.
@nl
type
label
Biochemical hallmarks of tyrosine hydroxylase deficiency.
@en
Biochemical hallmarks of tyrosine hydroxylase deficiency.
@nl
prefLabel
Biochemical hallmarks of tyrosine hydroxylase deficiency.
@en
Biochemical hallmarks of tyrosine hydroxylase deficiency.
@nl
P1433
P1476
P2093
P304
P31
P407
P433
P478
P577
P698
P1433
P1476
Biochemical hallmarks of tyrosine hydroxylase deficiency
@en
P2093
P304
P31
P407
P433
P478
P577
P698