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.
Čikaški stil citiranjaDE SILVA, R., R. PETTY, M. LOUDON, C. FREW, A. COOKE, i R. DAVIDSON. Molecular Genetic Diagnosis Of Friedreich's Ataxia in a Pedigree With Apparent Autosomal Dominant spinocerebellar Degeneration. BMJ Group, 1999.
MLA način citiranjaDE SILVA, R., et al. Molecular Genetic Diagnosis Of Friedreich's Ataxia in a Pedigree With Apparent Autosomal Dominant spinocerebellar Degeneration. BMJ Group, 1999.
Upozorenje: Ovi citati možda nisu uvijek 100% točni.