Publication

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

Journal: AMERICAN JOURNAL OF MEDICAL GENETICS PART A

ISSN: 1552-4825

Issue: 12

Volume: 167

Pages: 3214 - 3218

Publication year:2015

BOF-keylabel:yes

IOF-keylabel:yes

BOF-publication weight:0.1

CSS-citation score:1

Authors:International

Authors from:Higher Education

Accessibility:Closed