Facioscapulohumeral Muscular Dystrophy 1a

Overview of Facioscapulohumeral Muscular Dystrophy 1a

Most recent studies have shown that Facioscapulohumeral Muscular Dystrophy 1a shares some biological mechanisms with becker-muscular-dystrophy, cardiac-arrhythmia, childhood-soft-tissue-sarcoma, distal-muscular-dystrophies, dystrophy, embryonic-mosaic, facial-paresis, muscular-dystrophy, muscular-dystrophy-duchenne, muscular-dystrophy-facioscapulohumeral, myopathy, neoplasms, neuromuscular-diseases, polymyositis, rhabdomyosarcoma, rhabdomyosarcoma-embryonal, sarcoma, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Facioscapulohumeral Muscular Dystrophy 1a, and have been seen in publications frequently: Cell Death, Fertilization, Gene Conversion, Innervation, Localization, Oogenesis

Quite a number of genes have been found to play important roles in Facioscapulohumeral Muscular Dystrophy 1a, such as ACTN2, ALPP, ASRGL1, ATRNL1, CCL27, DMD, DUX4, EIF3K, EMD, EWSR1, FRG1, GDI1, MTSS1, NAT10, PDLIM3, PDLIM5, SLPI. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Facioscapulohumeral Muscular Dystrophy 1a Related Genes

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Pathways Related to Facioscapulohumeral Muscular Dystrophy 1a

This information is being compiled and will come in a future update

Related Diseases