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Three novel mutations, c314CA, C778insC, and c1285+2TA, in exon 2 of the Wilson disease gene

Authors :
J, Genschel
G, Sommer
R, Haas
C, Buettner
B, Bochow
M, Manns
H, Lochs
H H, Schmidt
Source :
Human mutation. 16(3)
Publication Year :
2000

Subjects

Subjects :
Adult
Mutagenesis, Insertional
Hepatolenticular Degeneration
Codon, Nonsense
Serine
Humans
RNA Splice Sites

Details

ISSN :
10981004
Volume :
16
Issue :
3
Database :
OpenAIRE
Journal :
Human mutation
Accession number :
edsair.pmid..........20dc023983eb591ca4400d82ded60653

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