Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome

Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome https://t.co/yqLAYNHO0l https://t.co/9GQfWOe9ft

Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome https://t.co/3oYuLmuicX

New Research: Identification of novel TMEM231 gene splice variants and pathological findings in a fetus with Meckel Syndrome: Background: Meckel Syndrome (MKS, OMIM #249000) is a rare and fatal autosomal recessive ciliopathy with high clinical… #Genetics h