Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.

Human mutation

Volumn 23, Issue 1, 2004, Pages 98-

  Sauter, S M ^a   Engel, W ^a   Neumann, L M ^a   Kunze, J ^a   Neesen, J ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GUANOSINE TRIPHOSPHATASE; SPG3A PROTEIN, HUMAN;

ADOLESCENT; ADULT; ARTICLE; CHILD; FEMALE; GENETIC LINKAGE; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; INFANT; MALE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; ONSET AGE; PEDIGREE; PRESCHOOL CHILD;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; GTP PHOSPHOHYDROLASES; HUMANS; INFANT; LINKAGE (GENETICS); MALE; MIDDLE AGED; MUTATION; PEDIGREE; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 1542783703     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9205     Document Type: Article

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