Primary hyperoxaluria type 1: Clinical, genetic, and evolutionary characteristics in Tunisian children

CONCLUSIONS: Screening for the disease would improve the prognosis of this condition.PMID:38445424

Source: Molecular Medicine - March 6, 2024 Category: Molecular Biology Authors: Abir Boussetta Rihab Fatnassi Manel Jellouli Rym Maamouri Ridha Mrad Tahar Gargah Asma Omezzine Source Type: research