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Paper Details

Mutations in RASA1 and GDF2 identified in patients with clinical features of hereditary hemorrhagic telangiectasia.
Hum Genome Var
48
2015
ACVRL1, ENG, GDF2, HHT, Hereditary hemorrhagic telangiectasia, RASA1, SMAD4, autosomal dominant vascular disorder, bone morphogenetic protein, dermal lesions, epistaxis, hereditary hemorrhagic telangiectasia, patients, telangiectases, transforming growth factor, vascular disorders

Datasets

Release 1.2