A distinct autosomal recessive ataxia maps to chromosome 12 in an inbred family from Jordan.
about
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndromeMutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans.Arranging marriage; negotiating risk: genetics and society in Qatar.The role of the cerebellum in the pathogenesis of cortical myoclonus
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A distinct autosomal recessive ataxia maps to chromosome 12 in an inbred family from Jordan.
description
2006 nî lūn-bûn
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name
A distinct autosomal recessive ...... an inbred family from Jordan.
@en
A distinct autosomal recessive ...... an inbred family from Jordan.
@nl
type
label
A distinct autosomal recessive ...... an inbred family from Jordan.
@en
A distinct autosomal recessive ...... an inbred family from Jordan.
@nl
prefLabel
A distinct autosomal recessive ...... an inbred family from Jordan.
@en
A distinct autosomal recessive ...... an inbred family from Jordan.
@nl
P2093
P2860
P50
P1476
A distinct autosomal recessive ...... n an inbred family from Jordan
@en
P2093
Ammar A Sadoon
Azhar Daoud
Ronald Spiegel
Suzanne M Leal
P2860
P304
P356
10.1016/J.BRAINDEV.2005.11.003
P577
2006-01-10T00:00:00Z