Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes. [electronic resource]
Producer: 20031007Description: 559-67 p. digitalISSN:- 0960-8966
- Adolescent
- Adult
- Aged
- Amino Acid Sequence
- Base Sequence
- Caenorhabditis elegans Proteins
- Carbohydrate Epimerases -- genetics
- Carrier Proteins -- genetics
- Chromosomes, Human, Pair 9
- DNA Mutational Analysis -- methods
- DNA, Recombinant
- Dementia -- complications
- Exons
- Genetic Heterogeneity
- Genetic Linkage
- Genetic Markers
- Humans
- Middle Aged
- Molecular Sequence Data
- Muscular Dystrophies -- complications
- Mutation
- Myositis, Inclusion Body -- complications
- NADH, NADPH Oxidoreductases -- genetics
- Nuclear Proteins -- genetics
- Osteitis Deformans -- complications
- Pedigree
- Phosphotransferases (Alcohol Group Acceptor) -- genetics
- RNA, Messenger -- biosynthesis
- Reverse Transcriptase Polymerase Chain Reaction -- methods
- Tropomyosin -- genetics
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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