C. Michielotto

SCA 28 , a novel form of autosomal dominant cerebellar ataxia on chromosome 18 p 11 . 22 – q 11 . 2

C. Gellera, A. Brusco, M. Grisoli, 2005 .

Large pathogenic expansions in the SCA2 and SCA7 genes can be detected by fluorescent repeat-primed polymerase chain reaction assay.

A. Durr, A. Brice, G. Stevanin, 2006, The Journal of molecular diagnostics : JMD.

Consultations in Molecular Diagnostics Large Pathogenic Expansions in the SCA2 and SCA7 Genes Can Be Detected by Fluorescent Repeat-Primed Polymerase Chain Reaction Assay

A. Durr, A. Brice, G. Stevanin, 2006 .

Detection of large pathogenic expansions in FRDA1, SCA10, and SCA12 genes using a simple fluorescent repeat-primed PCR assay.

T. Ashizawa, R. Margolis, C. Gellera, 2004, The Journal of molecular diagnostics : JMD.

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.

Franco Taroni, Caterina Mariotti, Alfredo Brusco, 2004, Archives of neurology.

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.

Marco Seri, Franco Taroni, Caterina Mariotti, 2006, Brain : a journal of neurology.

The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase γ gene is not associated with oligozoospermia

M. Zeviani, G. Matullo, A. Brusco, 2006, Journal of endocrinological investigation.