The only, remarkable exception was Filamin C (FLNC), which was found as a candidate on chromosome 7q for both the 608423 (limb-girdle muscular dystrophy type 1F) and the 603511 (limb-girdle muscular dystrophy type 1D) OMIM phenotype entries. Here, FLNC is linked to autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6).