NBEAL2 gene

Known as: NBEAL2, NEUROBEACHIN-LIKE 2, KIAA0540

National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.

2018

GPS (MIM 139090) is an autosomal recessive disorder associated with macrothrombocytopenia, splenomegaly, myelofibrosis…

2018

Gray platelet syndrome (GPS) is a rare, mostly autosomal recessive inherited platelet functional disorder with a mild to moderate…

2017

Mutations in NBEAL2 , the gene encoding the scaffolding protein Nbeal2 are causal of Gray Platelet Syndrome (GPS), a rare…