A Tunisian neonatal case of co-inheritance of G6PD...

Clinica Chimica Acta 2019 / 06 Vol. 493

A Tunisian neonatal case of co-inheritance of G6PD deficiency and HBC presenting as severe jaundice and hemolytic anemia

Dabboubi, R., Fredj, S. Hadj, Ghaffar, I. Ben, Siala, H., Boussetta, K., Messaoud, T.
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Volume:
493
Language:
english
Journal:
Clinica Chimica Acta
DOI:
10.1016/j.cca.2019.03.493
Date:
June, 2019
File:
PDF, 113 KB
english, 2019
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