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[A simple and rapid method for detection of the 106Gln mutation in Wilson-Konovalov disease].

Authors :
Shadrina MI
Slominskiĭ PA
Karabanov AV
Ivanova-Smolenskaia IA
Limborskaia SA
Source :
Genetika [Genetika] 2002 Dec; Vol. 38 (12), pp. 1723-5.
Publication Year :
2002

Abstract

A simple and rapid method for detecting the 1069Gln mutation in gene ATP7B based on a PCR specific for this allele has been developed. The 1069Gln mutation is the main cause of Wilson disease (WD) in Russia and accounts for approximately 40% of all mutant alleles of gene ATP7B. Therefore, the method proposed makes the postnatal and prenatal diagnosis of Wilson disease in Russia considerably more rapid and less expensive.

Details

Language :
Russian
ISSN :
0016-6758
Volume :
38
Issue :
12
Database :
MEDLINE
Journal :
Genetika
Publication Type :
Academic Journal
Accession number :
12575461