SCOPUS 정보 검색 플랫폼

Volumn 137, Issue 12, 2014, Pages e311-

Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

(10) Johnson, Janel O a Glynn, Shannon M a Raphael Gibbs, J a Nalls, Mike A a Sabatelli, Mario b Restagno, Gabriella c Drory, Vivian E d Chiò, Adriano e Rogaeva, Ekaterina f Traynor, Bryan J a

a NATIONAL INSTITUTE ON AGING (United States)

b CATHOLIC UNIVERSITY (Italy)

c REGINA MARGHERITA CHILDREN S HOSPITAL (Italy)

d Sourasky Medical Centre (Israel)

e UNIVERSITY OF TURIN (Italy)

f UNIVERSITY OF TORONTO (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AMYOTROPHIC LATERAL SCLEROSIS; CHCHD10 GENE; EXON; FAMILIAL DISEASE; GC RICH SEQUENCE; GENE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; HUMAN GENOME; LETTER; MUTATIONAL ANALYSIS; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; COMPLICATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; FEMALE; FRONTOTEMPORAL DEMENTIA; GENETICS; MALE; MITOCHONDRION; PATHOLOGY;

MITOCHONDRIAL DNA; MITOCHONDRIAL PROTEIN;

AMYOTROPHIC LATERAL SCLEROSIS; DNA, MITOCHONDRIAL; FEMALE; FRONTOTEMPORAL DEMENTIA; HUMANS; MALE; MITOCHONDRIA; MITOCHONDRIAL DISEASES; MITOCHONDRIAL PROTEINS;

EID: 84920873336 PISSN: 00068950 EISSN: 14602156 Source Type: Journal
DOI: 10.1093/brain/awu265 Document Type: Letter

Times cited : (112)

References (5)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.