TrialHuman genetics2020
Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans.
Mohammed Zain Seidahmed et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
10 papers cite it
this papercites it
TrialHuman genetics2020
Mohammed Zain Seidahmed et al.PubMed ↗Publisher ↗
No numbers read from the abstract.