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

PISACKA, M.; KRALOVA, M.; KRALOVA, J.; KORISTKA, M.; CERMAKOVA, Z.; HELLBERG, A.; HULT, A.; STORRY, J.R.; OLSSON, M.L. A new missense mutation in exon 7, c.662G>A, causing the Bw phenotype: a family study in Northern Moravia. Transfuze a hematologie dnes. 2016, roč. 22, č. S2, s. 48. ISSN 1213-5763.