Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-04-01
著者
-
Nagai Yoshitaka
Division Of Functional Genomics Department Of Post-genomics And Diseases Osaka University Graduate S
-
Toda Tatsushi
Division Of Clinical Genetics Department Of Medical Genetics Osaka University Graduate School Of Med
-
Sun Hao
The Department Of Medical Genetics Institute Of Medical Biology Chinese Academy Of Medical Sciences And Peking Union Medical College
-
Chu Jiayou
The Department Of Medical Genetics Institute Of Medical Biology Chinese Academy Of Medical Sciences And Peking Union Medical College
-
Fu Shouzhi
Emergency Department The Peoples Hospital Of Shiyan
-
SATAKE Wataru
Division of Neurology/Molecular Brain Science, Kobe University Graduate School of Medicine
-
ZHANG Changjun
Institute of Eugenics and Genetics
-
TIAN Youyong
Emergency Department, the Peoples Hospital of Shiyan
-
YU Jiankun
The Department of Medical Genetics, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College
-
QIAN Yaping
The Department of Medical Genetics, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College
-
QIAN Yuan
The Department of Medical Genetics, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College
-
Yu Jiankun
The Department Of Medical Genetics Institute Of Medical Biology Chinese Academy Of Medical Sciences And Peking Union Medical College
-
Qian Yuan
The Department Of Medical Genetics Institute Of Medical Biology Chinese Academy Of Medical Sciences And Peking Union Medical College
-
Nagai Yoshitaka
Division Of Neurology/molecular Brain Science Kobe University Graduate School Of Medicine
-
Qian Yaping
The Department Of Medical Genetics Institute Of Medical Biology Chinese Academy Of Medical Sciences And Peking Union Medical College
-
Toda Tatsushi
Division Of Neurology/molecular Brain Science Kobe University Graduate School Of Medicine
-
Satake Wataru
Division Of Neurology/molecular Brain Science Kobe University Graduate School Of Medicine
-
Tian Youyong
Emergency Department The Peoples Hospital Of Shiyan
関連論文
- LRRK2 P755L variant in sporadic Parkinson's disease
- Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
- Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases
- Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family
- Glycosylation in Congenital Muscular Dystrophies
- Fukuyama-type congenital muscular dystrophy (FCMD) and α-dystroglycanopathy
- Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia
- The genetic and molecular basis of muscular dystrophy : roles of cell-matrix linkage in the pathogenesis
- Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family
- Screening of genes involved in chromosome segregation during meiosis I : toward the identification of genes responsible for infertility in humans
- Screening of genes involved in chromosome segregation during meiosis I : in vitro gene transfer to mouse fetal oocytes
- Molecular pathology of Sandhoff disease with p.Arg505Gln in HEXB : application of simulation analysis