New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1

Annals of Neurology

Volumn 58, Issue 3, 2005, Pages 423-429

  Orlacchio, Antonio ^a,b   Kawarai, Toshitaka ^c   Gaudiello, Fabrizio ^b   St George Hyslop, Peter H ^c,d   Floris, Roberto ^b   Bernardi, Giorgio ^a,b  

^a IRCCS FONDAZIONE SANTA LUCIA   (Italy)

^b UNIVERSITY OF ROME TOR VERGATA   (Italy)

^c UNIVERSITY OF TORONTO   (Canada)

^d TORONTO WESTERN HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

SERINE PROTEINASE INHIBITOR; SORTING NEXIN 7; UNCLASSIFIED DRUG;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 1P; CHROMOSOME MAP; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; GENE; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC MARKER; HEARING IMPAIRMENT; HIATUS HERNIA; HUMAN; MALE; PEDIGREE; PRIORITY JOURNAL; PROTEIN TRANSPORT; SNX7 GENE; SPASTIC PARAPLEGIA; UNITED KINGDOM; VOMITING;

ADOLESCENT; ADULT; CARRIER PROTEINS; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; DATABASES, GENETIC; FAMILY HEALTH; FEMALE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; PEDIGREE; SPASTIC PARAPLEGIA, HEREDITARY; VESICULAR TRANSPORT PROTEINS;

EID: 24644469037     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20590     Document Type: Article

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