Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes.

Watts, Giles D J

Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes. [electronic resource] - Neuromuscular disorders : NMD Sep 2003 - 559-67 p. digital

Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

0960-8966

10.1016/s0960-8966(03)00070-1 doi


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