Insights into muscle degeneration from heritable inclusion body myopathies

Frontiers in Aging Neuroscience

Volumn 7, Issue FEB, 2015, Pages

  Krause, Sabine ^a  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

GNE myopathy; HNRNPA1; IBMPFD; Multisystem proteinopathy; VCP p97

Indexed keywords

ALPHA ACTININ 1; ALPHA ACTININ 3; HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN; HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN A1; HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN B1; HISTONE H2B; MYOSTATIN; PROTEIN P97; RNA BINDING PROTEIN; UNCLASSIFIED DRUG;

AUTOSOMAL DOMINANT INHERITANCE; DISEASE ASSOCIATION; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; FRONTOTEMPORAL DEMENTIA; GENE EXPRESSION; GENETIC CORRELATION; GENETIC SUSCEPTIBILITY; GNE MYOPATHY; HUMAN; INCLUSION BODY MYOPATHY; INCLUSION BODY MYOSITIS; MISSENSE MUTATION; MULTISYSTEM PROTEINOPATHY; MUSCLE ATROPHY; MYOPATHY; PAGET BONE DISEASE; PHENOTYPE; PROTEIN EXPRESSION; RNA METABOLISM; SARCOPENIA; SENESCENCE; SHORT SURVEY; SKELETAL MUSCLE;

EID: 84949117663     PISSN: None     EISSN: 16634365     Source Type: Journal    
DOI: 10.3389/fnagi.2015.00013     Document Type: Short Survey

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