Article
A novel compound heterozygous HAX1 mutation in a Chinese patient with severe congenital neutropenia and chronic myelomonocytic leukemia transformation but without neurodevelopmental abnormalities.
Haematologica - 1 Feb 2012
Xue Sheng-Li, Li Jin-Li, Zou Jing-Ying, Su Jian, Chen Su-Ning, Wu De-Pei
Abstract excerpt
No abstract is available from the source.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.