Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in Chinese patients with Wilson disease

Archives of Neurology

Volumn 58, Issue 6, 2001, Pages 971-976

  Wu, Zhi Ying ^a   Wang, Ning ^a   Lin, Min Ting ^a   Fang, Ling ^a   Murong, Shen Xing ^a   Yu, Long ^b  

^a FUJIAN MEDICAL UNIVERSITY   (China)

^b FUDAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; LEUCINE;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHINESE; CORRELATION FUNCTION; DNA DETERMINATION; FEMALE; GENE MUTATION; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; STATISTICAL ANALYSIS; WILSON DISEASE;

EID: 0034974763     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.58.6.971     Document Type: Article

References (24)

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19. Detection of subnanogram amounts of RNA in polyacrylamide gels in presence and absence of protein by staining with silver
20. Silver staining of DNA in polyacrylamide gels: Linearity and effect of fragment size
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24. Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant