Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias (Q34132338)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias |
scientific article |
Statements
1 reference
Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias (English)
1 reference
Alexandra Dürr
1 reference
Sylvie Forlani
1 reference
Cécile Zaros
1 reference
Claudia Cagnoli
1 reference
Patrizia Pappi
1 reference
Pascale Ribai
1 reference
Nicola Migone
1 reference
Isabelle Leber
1 reference
Alessandro Brussino
1 reference
Marco Barberis
1 reference
Russell L Margolis
1 reference
Susan E Holmes
1 reference
Marcello Nobili
1 reference
Sergio Padovan
1 reference
Luisa Pugliese
1 reference
Corrado Assalto
1 reference
1 October 2010
1 reference
1 reference
Identifiers
1 reference