Author:
Teh Bin Tean,Sullivan Alice-Ann,Farnebo Filip,Zander Cecilia,Li Fang Yuan,Strachan Noela,Schalling Martin,Larsson Catharina,Sandstrom Paul
Subject
Genetics(clinical),Genetics
Reference12 articles.
1. La myopathic oculaire au Canada Francais;Barbeau;Un Méd Can,1965
2. The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac α and β myosin heavy chain genes on chromosome 14q11.2-q13;Brais;Hum Mol Genet,1995a
3. Xie, Y, Tome FMS, Fardeau, Bouchard J-P, Rouleau GA. Strong linkage disequilibrium suggests one founder mutation is responsible for all cases of oculopharyngeal muscular dystrophy (OPMD) in the French Canadian population;Brais;Am J Hum Genet,1995b
4. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3prime; end of a transcript encoding a protein kinase family member;Brook;Cell,1992
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