Database for the mutations of the Finnish disease heritage.
Hum Mutat
; 19(1): 16-22, 2002 Jan.
Article
em En
| MEDLINE
| ID: mdl-11754099
ABSTRACT
The Finnish disease heritage refers to a group of monogenic diseases that are enriched in the Finnish population due to founder effect and genetic isolation. The molecular genetics of these diseases has recently been intensely studied, and several founder and private mutations have been identified. The purpose of the present study was to create a database of the presently known mutations of the Finnish disease heritage.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Bases de Dados Genéticas
/
Doenças Genéticas Inatas
/
Mutação
Tipo de estudo:
Etiology_studies
Limite:
Humans
País/Região como assunto:
Europa
Idioma:
En
Ano de publicação:
2002
Tipo de documento:
Article