Hereditary spastic paraplegia: Advances in genetic research

Neurology

Volumn 46, Issue 6, 1996, Pages 1507-1514

  Fink, J K ^a,i   Heiman Patterson, T ^b   Bird, T ^c   Cambi, F ^b   Dube M P ^e   Figlewicz, D A ^f   Haines, J L ^d   Hentati, A ^g   Pericak Vance, M A ^h   Raskind, W ^c   Rouleau, G A ^e   Siddique, T ^g  

^a UNIVERSITY OF MICHIGAN   (United States)

^b THOMAS JEFFERSON UNIVERSITY   (United States)

^c VETERANS AFFAIRS MEDICAL CENTER   (United States)

^d MASSACHUSETTS GENERAL HOSPITAL   (United States)

^e MONTREAL GENERAL HOSPITAL   (Canada)

^f UNIVERSITY OF ROCHESTER   (United States)

^g NORTHWESTERN UNIVERSITY   (United States)

^h DUKE UNIVERSITY MEDICAL CENTER   (United States)

ⁱ Med Science Research Building III ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; LIPOPROTEIN;

AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 14Q; CHROMOSOME 15Q; CHROMOSOME 2P; CHROMOSOME 8Q; DNA POLYMORPHISM; GENE LOCUS; GENE MUTATION; GENETIC COUNSELING; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; PRIORITY JOURNAL; REVIEW; X CHROMOSOME LINKED DISORDER;

EID: 8944250670     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.46.6.1507     Document Type: Review

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