A new missense mutation in exon 7, c.662G>A, causing the Bw phenotype: a family study in Northern Moravia

0011707 2017 CZ eng A
Písačka, Martin - Králová, Miroslava - Králová, Jana - Kořístka, M. - Čermáková, Z. - Hellberg, A. - Hult, A.K. - Storry, J.R. - Olsson, M.
A new missense mutation in exon 7, c.662G>A, causing the Bw phenotype: a family study in Northern Moravia.
Transfuze a hematologie dnes. Roč. 22, č. S2 (2016), s. 48. ISSN 1213-5763