A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy

por Naderi, Niloofar, Mohsen-Pour, Neda, Nilipour, Yalda, Pourirahim, Maryam, Maleki, Majid, Kalayinia, Samira
Publicado 2023

In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease

por Abbasi, Shiva, Mohsen-Pour, Neda, Naderi, Niloofar, Rahimi, Shahin, Maleki, Majid, Kalayinia, Samira
Publicado 2021