TY  - GEN
AU  - Watts,Giles D J
AU  - Thorne,M
AU  - Kovach,M J
AU  - Pestronk,A
AU  - Kimonis,Virginia E
TI  - Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes
SN  - 0960-8966
PY  - 2003///1007
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Amino Acid Sequence
KW  - Base Sequence
KW  - Caenorhabditis elegans Proteins
KW  - Carbohydrate Epimerases
KW  - genetics
KW  - Carrier Proteins
KW  - Chromosomes, Human, Pair 9
KW  - DNA Mutational Analysis
KW  - methods
KW  - DNA, Recombinant
KW  - Dementia
KW  - complications
KW  - Exons
KW  - Genetic Heterogeneity
KW  - Genetic Linkage
KW  - Genetic Markers
KW  - Humans
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Muscular Dystrophies
KW  - Mutation
KW  - Myositis, Inclusion Body
KW  - NADH, NADPH Oxidoreductases
KW  - Nuclear Proteins
KW  - Osteitis Deformans
KW  - Pedigree
KW  - Phosphotransferases (Alcohol Group Acceptor)
KW  - RNA, Messenger
KW  - biosynthesis
KW  - Reverse Transcriptase Polymerase Chain Reaction
KW  - Tropomyosin
N1  - Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1016/s0960-8966(03)00070-1
ER  -