Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia
| Image |  |
|---|---|
| Description | scientific article published on 10 September 2018 |
| Author/s |
author: Kanda Fanhchaksai Vorasuk Shotelersuk Pimlak Charoenkwan Fuanglada Tongprasert |
| Publication date | September 10, 2018 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |