LinkDB Search

PubMed

17336526             MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy. 
17439987             Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopath 
18179901             X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half 
21310615             Four and a half LIM protein 1 gene mutations cause four distinct human myopathies: a comprehensive r