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searching for Hereditary inclusion body myopathy 3 found (13 total)

alternate case: hereditary inclusion body myopathy

GNE (gene) (1,051 words) [view diff] exact match in snippet view article

Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, et al. (1996). "Hereditary inclusion body myopathy maps to chromosome 9p1-q1". Hum. Mol. Genet. 5 (1): 159–163

N-Acetylmannosamine (1,228 words) [view diff] case mismatch in snippet view article find links to article

sialic acid. The disease GNE myopathy [formerly known as hereditary Inclusion Body Myopathy (HIBM), and Distal Myopathy with Rimmed Vacuoles (DMRV)] is

N-acetyl-D-glucosamine kinase (880 words) [view diff] exact match in snippet view article find links to article

2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy". Glycobiology. 15 (11): 1102–10. doi:10.1093/glycob/cwi100