APA

Herman-Bert A., Stevanin G., Netter J. C., Rascol O., Brassat D., Calvas P., Camuzat A., Yuan Q., Schalling M., Dürr A. & Brice A. (20000807). Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation. : American journal of human genetics.

Chicago

Herman-Bert A, Stevanin G, Netter J C, Rascol O, Brassat D, Calvas P, Camuzat A, Yuan Q, Schalling M, Dürr A and Brice A. 20000807. Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation. : American journal of human genetics.

Harvard

Herman-Bert A., Stevanin G., Netter J. C., Rascol O., Brassat D., Calvas P., Camuzat A., Yuan Q., Schalling M., Dürr A. and Brice A. (20000807). Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation. : American journal of human genetics.

MLA

Herman-Bert A, Stevanin G, Netter J C, Rascol O, Brassat D, Calvas P, Camuzat A, Yuan Q, Schalling M, Dürr A and Brice A. Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation. : American journal of human genetics. 20000807.