Title: | Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype |
Journal : | European journal of human genetics, 19, 5 |
Authors: | Coenen MJH ; Tieleman AA ; Schijvenaars MMVAP ; Leferink M ; Ranum LPW ; Scheffer H ; van Engelen BGM |
Material Type: | Article |
Publication Date: | 2011 |
Size: | p. 567-570 |
Languages: | English |
Keywords : | chromosome 3 ; Europe (geography) ; founder effect ; gène ZNF9 ; genetic analysis ; genetic mutations ; genetic polymorphism ; haplotypes ; Morocco ; myotonic dystrophy type 2 ; Netherlands |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/pubmed/21224892 |
Pubmed / DOI : | DOI : 10.1038/ejhg.2010.233 |