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Neurological Research

Volumn 31, Issue 7, 2009, Pages 743-747

Familial and genetic researches on three Chinese families with von Hippel-Lindau disease

(5) Mao, Xiao Chun a Su, Zhi Peng a Yu, Wen Qiao a Zheng, Wei Ming a Zeng, Yan Jun b

a WENZHOU MEDICAL UNIVERSITY (China)

b BEIJING UNIVERSITY OF TECHNOLOGY (China)

Author keywords

CNS; Hemangioblastoma; VHL gene; Von Hippel Lindau disease

Indexed keywords

CYTOSINE; DNA; GUANINE; LEUCINE; SERINE; THREONINE; VALINE;

ADOLESCENT; ADULT; ARTICLE; BLOOD; CHINESE; CLINICAL ARTICLE; CLINICAL FEATURE; DATA BASE; DISEASE CARRIER; DISEASE COURSE; DISEASE SEVERITY; EXON; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HEMANGIOBLASTOMA; HUMAN; MALE; POLYMERASE CHAIN REACTION; VON HIPPEL LINDAU DISEASE;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; BRAIN NEOPLASMS; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HEMANGIOBLASTOMA; HUMANS; MALE; MIDDLE AGED; MUTATION; PHENOTYPE; RETROSPECTIVE STUDIES; SEVERITY OF ILLNESS INDEX; VON HIPPEL-LINDAU DISEASE; VON HIPPEL-LINDAU TUMOR SUPPRESSOR PROTEIN; YOUNG ADULT;

EID: 68849125012 PISSN: 01616412 EISSN: None Source Type: Journal
DOI: 10.1179/174313209X382421 Document Type: Article

Times cited : (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.