SCA2 trinucleotide expansion in German SCA patients
O Riess, FA Laccone, S Gispert, L Schöls, C Zühlke… - Neurogenetics, 1997 - Springer
Autosomal dominant spinocerebellar ataxias (SCA) are a group of clinically and genetically
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
[引用][C] SCA2 trinucleotide expansion in German SCA patients
O RIESS - Neurogenetics, 1997 - cir.nii.ac.jp
SCA2 trinucleotide expansion in German SCA patients
O Riess, FA Laccone, S Gispert, L Schöls… - …, 1997 - search.proquest.com
Autosomal dominant spinocerebellar ataxias (SCA) are a group of clinically and genetically
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
SCA2 trinucleotide expansion in German SCA patients
O Riess, F Laccone, S Gispert, L Schöls… - …, 1997 - epub.uni-regensburg.de
Autosomal dominant spinocerebellar ataxias (SCA) are a group of clinically and genetically
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
SCA2 trinucleotide expansion in German SCA patients
O Riess, FA Laccone, S Gispert, L Schls, C Zhlke… - neurogenetics, 1998 - infona.pl
Autosomal dominant spinocerebellar ataxias (SCA) are a group of clinically and genetically
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
SCA2 trinucleotide expansion in German SCA patients
O Riess, FA Laccone, S Gispert, L Schöls… - …, 1997 - research.uni-luebeck.de
Autosomal dominant spinocerebellar ataxias (SCA) are a group of clinically and genetically
heterogeneous neu rodegenerative disorders which lead to progressive cerebellar ataxia. A …
heterogeneous neu rodegenerative disorders which lead to progressive cerebellar ataxia. A …
SCA2 trinucleotide expansion in German SCA patients.
O Riess, FA Laccone, S Gispert, L Schöls, C Zühlke… - Neurogenetics, 1997 - europepmc.org
Autosomal dominant spinocerebellar ataxias (SCA) are a group of clinically and genetically
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
SCA2 trinucleotide expansion in German SCA patients
O Riess, FA Laccone, S Gispert, L Schöls… - …, 1997 - pubmed.ncbi.nlm.nih.gov
Autosomal dominant spinocerebellar ataxias (SCA) are a group of clinically and genetically
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
SCA2 trinucleotide expansion in German SCA patients
O Riess, FA Laccone, S Gispert, L Schols, C Zuhlke… - neurogenetics, 1997 - elibrary.ru
Autosomal dominant spinocerebellar ataxias (SCA) are a group of clinically and genetically
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
heterogeneous neurodegenerative disorders which lead to progressive cerebellar ataxia. A …
[引用][C] SCA2 trinucleotide expansion in German SCA patients
O Riess, FA Laccone, S Gispert, L Schöls, C Zühlke… - neurogenetics, 1997 - cir.nii.ac.jp
SCA2 trinucleotide expansion in German SCA patients | CiNii Research CiNii 国立情報学
研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 論文・データをさがす 大学 …
研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 論文・データをさがす 大学 …