Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis. [electronic resource]
Producer: 20171031Description: 1845-1856 p. digitalISSN:- 1528-0020
- Adult
- Anemia, Hemolytic, Congenital -- genetics
- Child
- Cohort Studies
- DNA Mutational Analysis
- Dehydration -- genetics
- Erythrocytes -- metabolism
- Family
- Female
- HEK293 Cells
- Humans
- Hydrops Fetalis -- genetics
- INDEL Mutation
- Infant, Newborn
- Ion Channels -- genetics
- Kinetics
- Male
- Mutation, Missense
- Osmotic Pressure -- physiology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
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