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Results 1 - 4 of 4 for fshd1
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  1. Facioscapulohumeral muscular dystrophy 
    ... two types of facioscapulohumeral muscular dystrophy: type 1 (FSHD1) and type 2 (FSHD2). The two types have ... people. About 95 percent of all cases are FSHD1; the remaining 5 percent are FSHD2. Facioscapulohumeral muscular ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  2. SMCHD1 gene 
    ... of the disorder have been described: type 1 (FSHD1) and type 2 (FSHD2). Changes in the SMCHD1 ... with the other type of facioscapulohumeral muscular dystrophy, FSHD1. FSHD1 results when the D4Z4 region is abnormally ...
    https://medlineplus.gov/genetics/gene/smchd1 - Genetics
  3. DUX4 gene 
    ... of the disorder have been described: type 1 (FSHD1) and type 2 (FSHD2). Both types result from ... has fewer methyl groups attached than normal. In FSHD1, hypomethylation occurs because the D4Z4 region is abnormally ...
    https://medlineplus.gov/genetics/gene/dux4 - Genetics
  4. Chromosome 4 
    ... groups attached. In facioscapulohumeral muscular dystrophy type 1 (FSHD1), hypomethylation occurs because the D4Z4 region contains between ...
    https://medlineplus.gov/genetics/chromosome/4 - Genetics