@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
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