Molecular genetic diagnosis of Friedreich's ataxia in a pedigree with apparent autosomal dominant spinocerebellar degeneration [5]

Journal of Neurology Neurosurgery and Psychiatry

Volumn 66, Issue 1, 1999, Pages 117-118

  De Silva, R ^a   Petty, R ^a   Loudon, M ^a   Frew, C ^a   Cooke, A ^a   Davidson, R ^a  

^a OLDCHURCH HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CEREBELLAR ATAXIA; CHROMOSOME 9; DEGENERATIVE DISEASE; FEMALE; FRIEDREICH ATAXIA; GENE MUTATION; HUMAN; INFANT; LETTER; MALE; MOLECULAR GENETICS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION;

ADULT; FEMALE; FRIEDREICH ATAXIA; HUMANS; MALE; PEDIGREE; SPINOCEREBELLAR DEGENERATIONS;

EID: 0032991537     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (3)