De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China

Neurobiology of Aging

Volumn 34, Issue 4, 2013, Pages 1312.e1-1312.e8

  Zou, Zhang Yu ^a   Cui, Li Ying ^a   Sun, Qing ^a   Li, Xiao Guang ^a   Liu, Ming Sheng ^a   Xu, Yan ^a   Zhou, Yan ^a   Yang, Xun Zhe ^a  

^a PEKING UNION MEDICAL COLLEGE HOSPITAL   (China)

Author keywords

Amyotrophic lateral sclerosis; FUS; Genetics; Juvenile onset

Indexed keywords

ARGININE; CYTOSINE; GLYCINE; GUANINE; LEUCINE; PROLINE; THYMINE; TRYPTOPHAN;

ADOLESCENT; ADULT; ADULT ONSET SPORADIC AMYOTROPHIC LATERAL SCLEROSIS; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CAUCASIAN; CHINESE; CONTROLLED STUDY; ETHNIC DIFFERENCE; ETHNIC GROUP; EXON; FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS; FEMALE; FRAMESHIFT MUTATION; FUS GENE; GENE; GENE DELETION; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; HETEROZYGOSITY; HUMAN; JAPANESE; JUVENILE ONSET SPORADIC AMYOTROPHIC LATERAL SCLEROSIS; KOREAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SOD1 GENE;

EID: 84872327415     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2012.09.005     Document Type: Article

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