Associated Papers
Directional next-generation RNA sequencing and examination of premature termination codon mutations in endoglin/hereditary haemorrhagic telangiectasia.
Govani FS et al.
Molecular Syndromology, 2013
High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients.
Schulte C et al.
Human Mutation, 2005
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