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المؤلفون: Alwazzan M; Institute of Genetics, University of Nottingham, Queen's Medical Centre, Nottingham NG7 2UH, UK., Newman E, Hamshere MG, Brook JD

المصدر: Human molecular genetics [Hum Mol Genet] 1999 Aug; Vol. 8 (8), pp. 1491-7.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Print ISSN: 0964-6906 (Print) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Cytoskeletal Proteins/*genetics , Membrane Proteins/*genetics , Myotonic Dystrophy/*genetics , Protein Serine-Threonine Kinases/*genetics , RNA/*metabolism , Trinucleotide Repeat Expansion/*genetics, Alleles ; Base Sequence ; Cell Line ; DNA/genetics ; Dystrophin-Associated Proteins ; Fibroblasts/cytology ; Fibroblasts/metabolism ; Homeodomain Proteins/genetics ; Humans ; Point Mutation ; Polymerase Chain Reaction ; Polymorphism, Genetic ; Polymorphism, Single-Stranded Conformational ; RNA/genetics