The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.
about
Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent triosThe gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originJapanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1Structure prediction of polyglutamine disease proteins: comparison of methods.Spinocerebellar ataxia 1 (SCA1) in the Japanese in Hokkaido may derive from a single common ancestryIsodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus.The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusTight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13Mapping of the gene for Machado-Joseph disease within a 3.6-cM interval flanked by D14S291/D14S280 and D14S81, on the basis of studies of linkage and linkage disequilibrium in 24 Japanese families.New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report.A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locusEffect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I.Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate regionA gene for episodic ataxia/myokymia maps to chromosome 12p13.Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.The inherited ataxias and the new genetics.High relative frequency of SCA1 in Poland reflecting a potential founder effect.Conserved sequence-tagged sites: a phylogenetic approach to genome mapping.
P2860
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P2860
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.
description
1991 nî lūn-bûn
@nan
1991 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
The gene for autosomal dominan ...... locus in three large kindreds.
@ast
The gene for autosomal dominan ...... locus in three large kindreds.
@en
type
label
The gene for autosomal dominan ...... locus in three large kindreds.
@ast
The gene for autosomal dominan ...... locus in three large kindreds.
@en
prefLabel
The gene for autosomal dominan ...... locus in three large kindreds.
@ast
The gene for autosomal dominan ...... locus in three large kindreds.
@en
P2093
P2860
P1476
The gene for autosomal dominan ...... locus in three large kindreds.
@en
P2093
A E McCall
L A Sandkuijl
S A Huntoon
T J Kwiatkowski
P2860
P407
P50
P577
1991-07-01T00:00:00Z