The silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype

American Journal of Human Genetics

Volumn 69, Issue 1, 2001, Pages 209-215

  Patel, H ^a   Hart, P E ^b   Warner, T T ^b   Houlston, R S ^c   Patton, M A ^a   Jeffery, S ^a   Crosby, A H ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^b ROYAL FREE HOSPITAL   (United Kingdom)

^c INSTITUTE OF CANCER RESEARCH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 11Q; CLINICAL ARTICLE; DEGENERATIVE DISEASE; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC MARKER; HAND MUSCLE; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MUSCLE ATROPHY; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME;

EID: 0034969438     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/321267     Document Type: Article

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