SCOPUS 정보 검색 플랫폼

Nature Neuroscience

Volumn 18, Issue 5, 2015, Pages 611-613

Exome sequencing uncovers hidden pathways in familial and sporadic ALS

(2) Bettencourt, Conceição a Houlden, Henry a

a UNIVERSITY COLLEGE LONDON (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMYOTROPHIC LATERAL SCLEROSIS; AUTOPHAGY; EXOME; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HEREDITY; HUMAN; NERVOUS SYSTEM INFLAMMATION; PRIORITY JOURNAL; SHORT SURVEY; BIOLOGICAL MODEL; DNA SEQUENCE; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETICS; MISSENSE MUTATION; PHYSIOLOGY;

COPPER ZINC SUPEROXIDE DISMUTASE; PROTEIN SERINE THREONINE KINASE; SUPEROXIDE DISMUTASE; TBK1 PROTEIN, HUMAN;

AMYOTROPHIC LATERAL SCLEROSIS; EXOME; GENETIC HETEROGENEITY; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MODELS, GENETIC; MUTATION, MISSENSE; PROTEIN-SERINE-THREONINE KINASES; SEQUENCE ANALYSIS, DNA; SUPEROXIDE DISMUTASE;

EID: 84936751681 PISSN: 10976256 EISSN: 15461726 Source Type: Journal
DOI: 10.1038/nn.4012 Document Type: Short Survey

Times cited : (24)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.