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

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Description scientific article published on 11 September 2015
Author/s

author: Frank Kooy  Amos J Simon  Victoria Bordon  Raz Somech  Ilse Meerschaut  Bert Callewaert 

Publication date September 11, 2015
Language English
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