Missense C168T in the Wiskott–Aldrich Syndrome protein gene is a common mutation in X-linked thrombocytopenia
Lye Lin Ho, Juliet Ayling, Ian Prosser, Harry Kronenberg, Harry Iland, Douglas JoshuaVolume:
112
Year:
2001
Language:
english
Pages:
5
DOI:
10.1046/j.1365-2141.2001.02465.x
File:
PDF, 170 KB
english, 2001