Whole-exome sequencing as first-tier testing approach for identification of the causal mutations in hereditary spherocytosis candidate genes and the use of non-sanger-based methods for validation of the findings
Camila, N., Rita, T. Santa, Mesquita, P., Jácomo, R., Nery, L., Barra, G.Volume:
493
Language:
english
Journal:
Clinica Chimica Acta
DOI:
10.1016/j.cca.2019.03.963
Date:
June, 2019
File:
PDF, 83 KB
english, 2019