Homozygous missense and nonsense mutations in BMPR1B cause...

European Journal of Human Genetics 2014 / 6 Vol. 22; Iss. 6

Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe

Graul-Neumann, Luitgard M, Deichsel, Alexandra, Wille, Ulrike, Kakar, Naseebullah, Koll, Randi, Bassir, Christian, Ahmad, Jamil, Cormier-Daire, Valerie, Mundlos, Stefan, Kubisch, Christian, Borck, Gun
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Volume:
22
Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2013.222
Date:
June, 2014
File:
PDF, 2.21 MB
english, 2014
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