Associated Papers
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.
Ravenscroft TA et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.
Cox TC et al.
Human Mutation, 2019
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