[1]
Jini, P. and Tani, T. trans. 2026. Familial hypercholanemia Type 1 with associated glucose 6 phosphate dehydrogenase deficiency presenting with acute liver failure in the immediate newborn period. Indian Journal of Case Reports. 12, 6 (Jun. 2026), 395–398. DOI:https://doi.org/10.32677/ijcr.v12i6.8214.