论文信息 - Severe congenital neutropenia with neurological impairment due to a homozygous VPS45 p.E238K mutation: A case report suggesting a genotype–phenotype correlation - 字舞流文

Severe congenital neutropenia with neurological impairment due to a homozygous VPS45 p.E238K mutation: A case report suggesting a genotype–phenotype correlation

C. Klein | A. Simon | R. Kooy | R. Somech | A. Vanlander | B. Callewaert | C. Dhooge | Ilse Meerschaut | V. Bordon | P. Delbeke