Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the...

por Gholizadeh, Mehdi Agha, Mohammadi-Sarband, Mina, Fardanesh, Fatemeh, Garshasbi, Masoud
Publicado 2022