A locus for autosomal dominant 'pure' hereditary spastic paraplegia maps to chromosome 19q13

American Journal of Human Genetics

Volumn 66, Issue 2, 2000, Pages 728-732

  Reid, E ^a   Dearlove, A M ^b   Osborn, O ^b   Rogers, M T ^c   Rubinsztein, D C ^a,d  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b MEDICAL RESEARCH COUNCIL   (United Kingdom)

^c CARDIFF UNIVERSITY   (United Kingdom)

^d UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 19Q; CHROMOSOME MAP; CLINICAL ARTICLE; GENE LOCUS; GENETIC LINKAGE; HAPLOTYPE; HUMAN; PRIORITY JOURNAL; SCORING SYSTEM; SPASTIC PARAPLEGIA;

EID: 0033912569     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302783     Document Type: Article

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