Very high frequency of the His1069Gln mutation in Polish Wilson disease patients
J Neurol
.
1997 Sep;244(9):591-2.
doi: 10.1007/s004150050149.
Authors
A Czlonkowska
,
M Rodo
,
J Gajda
,
H K Ploos van Amstel
,
J Juyn
,
R H Houwen
PMID:
9352458
DOI:
10.1007/s004150050149
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
MeSH terms
Adolescent
Adult
Amino Acid Substitution*
Hepatolenticular Degeneration / genetics*
Histidine*
Humans
Point Mutation*
Poland
Substances
Histidine