Phenotypes in Swiss patients with familial ALS carrying TARDBP mutations

Neurodegenerative Diseases

Volumn 12, Issue 3, 2013, Pages 150-155

  Czell, D ^a   Andersen, P M ^d   Morita, M ^e   Neuwirth, C ^a   Perren, F ^b   Weber, M ^a,c  

^a Neuromuscular Diseases Unit   (Switzerland)

^b GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^c UNIVERSITY HOSPITAL BASEL   (Switzerland)

^d UMEÅ UNIVERSITY   (Sweden)

^e JICHI MEDICAL UNIVERSITY   (Japan)

Author keywords

Amyotrophic lateral sclerosis; Genetic counseling; Mutation; Phenotype; TARDBP

Indexed keywords

ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CLINICAL FEATURE; COGNITIVE DEFECT; DISEASE COURSE; FAMILY HISTORY; FEMALE; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC COUNSELING; GENETIC SCREENING; HUMAN; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; SOD1 GENE; SURVIVAL RATE; TARDBP GENE; CLINICAL ARTICLE; DISEASE PREDISPOSITION; FAMILY; SIBLING; SURVIVAL; SWISS;

TAR DNA BINDING PROTEIN;

EID: 84884289442     PISSN: 16602854     EISSN: 16602862     Source Type: Journal    
DOI: 10.1159/000345835     Document Type: Article

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