The other mutation is found: follow-up of an exceptional family with Wilson disease
Am J Gastroenterol
.
2004 Dec;99(12):2504-5.
doi: 10.1111/j.1572-0241.2004.41389_8.x.
Authors
Gabor Firneisz
,
Laszlo Szonyi
,
Peter Ferenci
,
Claudia Willheim
,
Andrea Horvath
,
Aniko Folhoffer
,
Zsolt Tulassay
,
Ferenc Szalay
PMID:
15571607
DOI:
10.1111/j.1572-0241.2004.41389_8.x
No abstract available
Publication types
Comment
Letter
MeSH terms
Hepatolenticular Degeneration / genetics*
Humans
Mutation, Missense*
Pedigree