Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutation in 6/16 Flamish families with breast and/or ovarian cancer but not in 12 sporadic patinets with early-onset disease

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F99%3A00000010" target="_blank" >RIV/00209805:_____/99:00000010 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutation in 6/16 Flamish families with breast and/or ovarian cancer but not in 12 sporadic patinets with early-onset disease

Original language description

As the mutational spectrum of the BRCA1 and BRCA2 genes in Belgium population is largely unknown, there was initiated mutation analysis for the complete coding sequence of both genes in Belgian families with multiple breast and/or ovarian cancer patientsand in "sporadic" patients with early onset disease. Disease causing mutation was found in 6/16 Flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

EB - Genetics and molecular biology

OECD FORD branch

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Project

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Continuities

Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

1999

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Human Mutation

ISSN

1059-7794

e-ISSN

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Volume of the periodical

13

Issue of the periodical within the volume

neuv.

Country of publishing house

US - UNITED STATES

Number of pages

3

Pages from-to

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UT code for WoS article

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EID of the result in the Scopus database

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