Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis

Journal of the Neurological Sciences

Volumn 317, Issue 1-2, 2012, Pages 58-61

  Praline, Julien ^a,b   Blasco, Hélène ^a,c   Vourc'H, Patrick ^a,c   Rat, Valérian ^a,c   Gendrot, Chantal ^c   Camu, William ^d   Andres, Christian R ^a,c  

^a UNIVERSITÉ DE TOURS   (France)

^b UNIVERSITY HOSPITAL OF TOURS   (France)

^c CHU BRETONNEAU   (France)

^d GUI DE CHAULIAC HOSPITAL   (France)

Author keywords

Amyotrophic lateral sclerosis; Genetic association study; Genetics; Hemochromatosis

Indexed keywords

HFE PROTEIN;

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CONTROLLED STUDY; DISEASE DURATION; FEMALE; GENDER; GENE FREQUENCY; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PRIORITY JOURNAL; SPORADIC AMYOTROPHIC LATERAL SCLEROSIS;

ADULT; AGED; AGED, 80 AND OVER; AMYOTROPHIC LATERAL SCLEROSIS; COHORT STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; FRANCE; GENE FREQUENCY; HISTOCOMPATIBILITY ANTIGENS CLASS I; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; POLYMORPHISM, GENETIC; SINGLE-BLIND METHOD; YOUNG ADULT;

EID: 84860295052     PISSN: 0022510X     EISSN: 18785883     Source Type: Journal    
DOI: 10.1016/j.jns.2012.02.029     Document Type: Article

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