[Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis].

Subjects

Subjects :

Fragile X Mental Retardation Protein
Fragile X Syndrome diagnosis
Genetic Carrier Screening
Humans
Male
Structure-Activity Relationship
Fragile X Syndrome genetics
Nerve Tissue Proteins isolation & purification
RNA-Binding Proteins isolation & purification

Details

Language :

Finnish

ISSN :

0012-7183

Volume :

108

Issue :

17

Database :

MEDLINE

Journal :

Duodecim; laaketieteellinen aikakauskirja

Publication Type :

Editorial & Opinion

Accession number :

1366164