Wilson disease in two consecutive generations: an exceptional family
Am J Gastroenterol
.
2001 Jul;96(7):2269-71.
doi: 10.1111/j.1572-0241.2001.03983.x.
Authors
G Firneisz
,
L Szönyi
,
P Ferenci
,
D Görög
,
B Nemes
,
F Szalay
PMID:
11467673
DOI:
10.1111/j.1572-0241.2001.03983.x
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Adolescent
Adult
Child
Family Health
Female
Hepatolenticular Degeneration / genetics*
Humans
Male
Pedigree
Point Mutation