Find link

language:

Find link is a tool written by Edward Betts.

Longer titles found: Sporadic late-onset nemaline myopathy (view)

searching for Nemaline myopathy 5 found (30 total)

TNNT1 (1,998 words) [view diff] exact match in snippet view article find links to article

exon 11 of TNNT1 gene causes Amish Nemaline Myopathy (ANM), which is a severe form of recessive nemaline myopathy originally found in the Old Order Amish

Tropomyosin 3 (888 words) [view diff] exact match in snippet view article find links to article

actin filament. Mutations in this gene result in autosomal dominant nemaline myopathy, and oncogenes formed by chromosomal translocations involving this

Actin, alpha skeletal muscle (1,505 words) [view diff] exact match in snippet view article find links to article

Mutations in the ACTA1 gene are known to cause the following conditions: Nemaline myopathy 3 (NEM3); Myopathy, actin, congenital, with excess of thin myofilaments

SBK3 (2,118 words) [view diff] exact match in snippet view article find links to article

and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy". Human Molecular Genetics. 24 (18): 5219–33. doi:10.1093/hmg/ddv243

Tropomyosin (6,192 words) [view diff] exact match in snippet view article find links to article

high antigenicity of tropomyosins released from compromised cells. Nemaline myopathy is a muscle disease that is characterised by the presence of electron-dense