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Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1
Heimdal, K., Dalhus, B., Rødningen, O.K., Kroken, M., Eiklid, K., Dheyauldeen, S., Røysland, T., Andersen, R., Kulseth, M.A.Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12612
Date:
June, 2015
File:
PDF, 426 KB
english, 2015