Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.

Human mutation

Volumn 30, Issue 2, 2009, Pages

  Goizet, Cyril ^a   Boukhris, Amir ^a   Mundwiller, Emeline ^a   Tallaksen, Chantal ^a   Forlani, Sylvie ^a   Toutain, Annick ^a   Carriere, Nathalie ^a   Paquis, Véronique ^a   Depienne, Christel ^a   Durr, Alexandra ^a   Stevanin, Giovanni ^a   Brice, Alexis ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

KIF5A PROTEIN, HUMAN; KINESIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; FEMALE; GENE FREQUENCY; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MIDDLE AGED; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRESCHOOL CHILD;

ADOLESCENT; ADULT; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; HUMANS; KINESIN; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 64049111042     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.20920     Document Type: Article

References (0)