Nasim Rahmani
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Publications (1)
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|Sep 10, 2021
Familial Hypomagnesemia with Hypercalciuria, Nephrocalcinosis, and Bilateral Chorioretinal Atrophy in a Patient with Homozygous p.G75S Variant in CLDN19.Nasim Rahmani, Saeed Talebi, Nakysa Hooman
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