Activity

Filter

Cancel
Date Panel Item Activity
4 actions
Congenital myopathy v3.69 MYH14 Arina Puzriakova Phenotypes for gene: MYH14 were changed from ?Peripheral neuropathy, myopathy, hoarseness, and hearing loss 614369; Deafness, autosomal dominant 4A 600652 to ?Peripheral neuropathy, myopathy, hoarseness, and hearing loss, OMIM:614369
Congenital myopathy MYH14 Anna Sarkozy reviewed MYH14
Congenital myopathy MYH14 Helen Brittain marked MYH14 as ready
Congenital myopathy MYH14 Helen Brittain reviewed MYH14