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Issue Date
Title
Author(s)
2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Hirata, H.
;
McMichael, G.
;
Haan, E.
;
MacLennan, A.
;
Yap, T.
;
Nguyen, L.
;
Shaw, M.
;
Gecz, J.
2013
NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsy
McMichael, G.
;
Haan, E.
;
Gardner, A.
;
Yap, T.
;
Thompson, S.
;
Ouvrier, R.
;
Dale, R.
;
Gecz, J.
;
MacLennan, A.
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Author
2
Gecz, J.
2
Haan, E.
2
MacLennan, A.
2
McMichael, G.
1
Dale, R.
1
Gardner, A.
1
Hirata, H.
1
Nguyen, L.
1
Ouvrier, R.
1
Shaw, M.
.
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Subject
1
Abnormalities, Multiple
1
Animals
1
Arthrogryposis
1
Ataxic cerebral palsy
1
Benign hereditary chorea
1
Carrier Proteins
1
Cells, Cultured
1
Chromosome Breakpoints
1
Comparative Genomic Hybridization
1
Dyskinetic cerebral palsy
.
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Date issued
2
2013