DE SILVA, R., PETTY, R., LOUDON, M., FREW, C., COOKE, A., & DAVIDSON, R. (1999). Molecular genetic diagnosis of Friedreich's ataxia in a pedigree with apparent autosomal dominant spinocerebellar degeneration. BMJ Group.
Chicago Style aipamenaDE SILVA, R., R. PETTY, M. LOUDON, C. FREW, A. COOKE, and R. DAVIDSON. Molecular Genetic Diagnosis Of Friedreich's Ataxia in a Pedigree With Apparent Autosomal Dominant spinocerebellar Degeneration. BMJ Group, 1999.
MLA aipamenaDE SILVA, R., et al. Molecular Genetic Diagnosis Of Friedreich's Ataxia in a Pedigree With Apparent Autosomal Dominant spinocerebellar Degeneration. BMJ Group, 1999.
Kontuz: berrikusi erreferentzia hauek erabili aurretik.