Associated Papers
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.
AitRaise I et al.
Biochemical Genetics, 2024
Lessons learned from the real-world diagnosis and management of hereditary hypophosphatemic rickets.
Chaturvedi D et al.
Bone Reports, 2024
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1.
Enerbäck S et al.
Journal of the American Society of Nephrology : Jasn, 2018
Familial acidosis of renal tubular origin.
WILANSKY DL et al.
Canadian Medical Association Journal, 1960
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