A novel mutation in the HIF prolyl hydroxylase, PHD2, associated with familial erythrocytosis

Autoria(s): Percy, M.J.; Zhao, Q.; Floresw, A.; Harrisonz, C.; Lappin, Terence; Maxwell, P.H.; McMullin, Mary Frances; Lee, F.S.
Data(s)

01/04/2006
Identificador

http://pure.qub.ac.uk/portal/en/publications/a-novel-mutation-in-the-hif-prolyl-hydroxylase-phd2-associated-with-familial-erythrocytosis(bcdc50a0-ac68-4133-bc74-bd7078f4c7aa).html
Idioma(s)

eng
Direitos

info:eu-repo/semantics/restrictedAccess
Fonte

Percy , M J , Zhao , Q , Floresw , A , Harrisonz , C , Lappin , T , Maxwell , P H , McMullin , M F & Lee , F S 2006 , ' A novel mutation in the HIF prolyl hydroxylase, PHD2, associated with familial erythrocytosis ' British Journal of Haematology , vol 133 , pp. 16-16 .
Tipo

article
Acesso ao item digital