Autosomal recessive hereditary spastic paraplegia - Clinical and genetic characteristics of a well-defined cohort

Neurogenetics

Volumn 14, Issue 3-4, 2013, Pages 181-188

  Yoon, G ^a   Baskin, B ^a,f   Tarnopolsky, M ^b   Boycott, K M ^c   Geraghty, M T ^c   Sell, E ^c   Goobie, S ^d   Meschino, W ^e   Banwell, B ^a   Ray, P N ^a,g  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b MCMASTER UNIVERSITY   (Canada)

^c CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^d LONDON HEALTH SCIENCES CENTRE   (Canada)

^e NORTH YORK GENERAL HOSPITAL   (Canada)

^f UPPSALA UNIVERSITY   (Sweden)

^g UNIVERSITY OF TORONTO   (Canada)

Author keywords

Ataxia; Genetics; Spastic paraplegia

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CANADA; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COHORT ANALYSIS; FEMALE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HUMAN; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NUCLEOTIDE SEQUENCE; PNPLA6 GENE; PRIORITY JOURNAL; PYRAMIDAL TRACT; SPASTIC PARAPLEGIA; SPG11 GENE; SPG7 GENE; ZFYVE26 GENE;

ADOLESCENT; ADULT; AGED; CHILD; COHORT STUDIES; FEMALE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; MIDDLE AGED; MUTATION; PYRAMIDAL TRACTS; SPASTIC PARAPLEGIA, HEREDITARY; YOUNG ADULT;

EID: 84888033187     PISSN: 13646745     EISSN: 13646753     Source Type: Journal    
DOI: 10.1007/s10048-013-0366-9     Document Type: Article

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