Associated Papers
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC et al.
Nature Genetics, 2020
32989326 (PubMed )
Supplement: 41588_2020_695_MOESM3_ESM.xlsx › Data_set_1
Myosins and Disease.
Coluccio LM
Advances in Experimental Medicine and Biology, 2020
Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families.
Baek JI et al.
Orphanet Journal of Rare Diseases, 2012
Are MYO1C and MYO1F associated with hearing loss?
Zadro C et al.
Biochimica Et Biophysica Acta, 2009
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