(Q46907223)
Statements
Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene (English)
N Ishikawa
M Miki
K Shirao
H Kihara
M Tsumura
K Nakamura
H Kawaguchi
S Yasunaga
K Matsubara
M Sako
J Hara
M Shiohara
S Kojima
T Sato
Y Takihara