Supplementary MaterialsDocument S1. causative mutations in these genes, specifically those that have been positionally mapped by genetic linkage studies. When hearing impairment occurs as part of a genetic syndrome, candidate genes can usually be identified on the basis of a hypothesized function consistent with the physiological effects of the syndrome or by the correlation of… Continue reading Supplementary MaterialsDocument S1. causative mutations in these genes, specifically those that
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Myotonic dystrophy type 2 (DM2) is definitely a dominantly inherited autosomal
Myotonic dystrophy type 2 (DM2) is definitely a dominantly inherited autosomal disease with multi-systemic Rivaroxaban Diol medical features and it is caused by expansion of a CCTG tetranucleotide repeat in the 1st intron of the zinc finger protein 9 (ZNF9) gene in 3q21. at fluorescence and transmission electron microscopy by using a panel of antibodies… Continue reading Myotonic dystrophy type 2 (DM2) is definitely a dominantly inherited autosomal