Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental …
T Matilla, V Volpinl, D Genis, J Rosell… - Human molecular …, 1993 - academic.oup.com
Autosomal dominant cerebellar ataxia type 1 (ADCA1) is a clinical and genetic
heterogeneous neurodegenerative disorder which leads to progressive cerebellar ataxia …
heterogeneous neurodegenerative disorder which leads to progressive cerebellar ataxia …
[引用][C] Presymptomatic analysis of spinocerebrllar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG repeat in a large pedigree displaying anticipation and …
T MATILLA - Hum Mol Genet, 1993 - cir.nii.ac.jp
Presymptomatic analysis of spinocerebrllar ataxia type 1 (SCA1) via the expansion of the
SCA1 CAG repeat in a large pedigree displaying anticipation and parental male bias | CiNii …
SCA1 CAG repeat in a large pedigree displaying anticipation and parental male bias | CiNii …
Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental …
T Matilla, V Volpini, D Genís, J Rosell… - Human molecular …, 1993 - pubmed.ncbi.nlm.nih.gov
Autosomal dominant cerebellar ataxia type 1 (ADCA1) is a clinical and genetic
heterogeneous neurodegenerative disorder which leads to progressive cerebellar ataxia …
heterogeneous neurodegenerative disorder which leads to progressive cerebellar ataxia …
Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental …
T Matilla, V Volpini, D Genís, J Rosell… - Human Molecular …, 1993 - europepmc.org
Autosomal dominant cerebellar ataxia type 1 (ADCA1) is a clinical and genetic
heterogeneous neurodegenerative disorder which leads to progressive cerebellar ataxia …
heterogeneous neurodegenerative disorder which leads to progressive cerebellar ataxia …
Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental …
T Matilla, V Volpinl, D Genis, J Rosell, J Corral… - Human Molecular …, 1993 - elibrary.ru
Autosomal dominant cerebellar ataxia type 1 (ADCA1) is a clinical and genetic
heterogeneous neurodegenerative disorder which leads to progressive cerebellar ataxia …
heterogeneous neurodegenerative disorder which leads to progressive cerebellar ataxia …
[引用][C] Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and …
T MATILLA, V VOLPINI, D GENIS… - Human molecular …, 1993 - pascal-francis.inist.fr
Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the
SCA1 CAG-repeat in a large pedigree displaying anticipation and parental male bias CNRS …
SCA1 CAG-repeat in a large pedigree displaying anticipation and parental male bias CNRS …