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New Congenital Neutropenia Syndrome And Causative Gene Mutation Identified By Scientists

Jan 6th, 2009 | By buddy1 | Category: Children's Health, Health & Wellness News

A team of scientists has discovered a new syndrome associated with severe congenital neutropenia (SCN), a rare disorder in which children lack sufficient infection-fighting white cells, and identified the genetic cause of the syndrome: mutations in the gene Glucose-6-phosphatase, catalytic subunit 3 (G6PC3). The findings, which are published in the Jan.

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