Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene.

Human mutation

Volumn 21, Issue 2, 2003, Pages 170-

  Proukakis, C ^a   Auer Grumbach, M ^a   Wagner, K ^a   Wilkinson, P A ^a   Reid, E ^a   Patton, M A ^a   Warner, T T ^a   Crosby, A H ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; SPAST PROTEIN, HUMAN;

ARTICLE; CHEMISTRY; CLINICAL TRIAL; EXON; GENE DUPLICATION; GENETIC SCREENING; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; INTRON; LEUKOCYTE; METHODOLOGY; MULTICENTER STUDY; MUTATION;

ADENOSINE TRIPHOSPHATASES; EXONS; GENE DUPLICATION; GENETIC SCREENING; HUMANS; INTRONS; LEUKOCYTES; MUTATION; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 0037313655     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9108     Document Type: Article

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