@radiomother15
Active 3 years, 9 months ago
A manuscript heterozygous NKX2-5 mutation, p.P59A, was recognized inside a family using autosomal dominating inherited VSD. Missing from the 190 handle people, the mutation has been extremely conserved evolutionarily and co-segregated along with VSD in the family using complete penetrance. Functional analysis said that the particular p.P59A […] View
Events
Events I'm Attending
Not attending any events yet.

