A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.
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Benign Hereditary Chorea: An UpdateBenign hereditary chorea related to NKX2-1 with ataxia and dystoniaRecent advances in genetics of choreaMurine hypothalamic destruction with vascular cell apoptosis subsequent to combined administration of human papilloma virus vaccine and pertussis toxin.Reliability of phenotypic early-onset ataxia assessment: a pilot study.Resistance to thyrotropin.A Methylome-Wide Association Study of Trajectories of Oppositional Defiant Behaviors and Biological Overlap With Attention Deficit Hyperactivity Disorder.NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement
P2860
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P2860
A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.
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2014 nî lūn-bûn
@nan
2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
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2014年学术文章
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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
name
A novel de novo mutation of th ...... and review of the literature.
@ast
A novel de novo mutation of th ...... and review of the literature.
@en
A novel de novo mutation of th ...... and review of the literature.
@nl
type
label
A novel de novo mutation of th ...... and review of the literature.
@ast
A novel de novo mutation of th ...... and review of the literature.
@en
A novel de novo mutation of th ...... and review of the literature.
@nl
prefLabel
A novel de novo mutation of th ...... and review of the literature.
@ast
A novel de novo mutation of th ...... and review of the literature.
@en
A novel de novo mutation of th ...... and review of the literature.
@nl
P2093
P2860
P50
P921
P1433
P1476
A novel de novo mutation of th ...... y and review of the literature
@en
P2093
Kailash P Bhatia
Marina Frontali
Michael H Parkinson
P2860
P2888
P304
P356
10.1007/S12311-014-0570-7
P577
2014-10-01T00:00:00Z
P5875
P6179
1000472027