Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia

Neurogenetics

Volumn 3, Issue 2, 2001, Pages 91-97

  Ashley Koch, Allison ^a   Bonner, Erin R ^a   Gaskell, P Craig ^a   West, Sandra G ^a   Tim, Richard ^a   Wolpert, Chantelle M ^a   Jones, Rodney ^a   Farrell, Carolyn D ^b   Nance, Martha ^c   Svenson, Ingrid K ^a   Marchuk, Douglas A ^a   Boustany, Rose Mary N ^a   Vance, Jeffery M ^a   Scott, William K ^a   Pericak Vance, Margaret A ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b ROSWELL PARK CANCER INSTITUTE   (United States)

^c Struthers Parkinson Center   (United States)

Author keywords

Autosomal dominant familial spastic paraplegia; Chromosome 12q; Chromosome 19q; Linkage

Indexed keywords

ARTICLE; CHROMOSOME 12; CHROMOSOME 19; CHROMOSOME 2; CHROMOSOME 8; CHROMOSOME MAP; DOMINANT GENE; FEMALE; GENETIC LINKAGE; GENETIC MARKER; GENETICS; GENOTYPE; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; PEDIGREE;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; GENES, DOMINANT; GENETIC MARKERS; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; PEDIGREE; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 18044401375     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100480000098     Document Type: Article

References (18)

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