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Hereditary kidney diseases associated with hypomagnesemia
Felix Claverie-Martin, Ana Perdomo-Ramirez, Victor Garcia-Nieto
Kidney Res Clin Pract. 2021;40(4):512-526.   Published online November 12, 2021
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Original Articles
PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data
Mona Entezam, Mohammad Reza Khatami, Fereshteh Saddadi, Mohsen Ayati, Jamshid Roozbeh, Mohammad Keramatipour
Kidney Res Clin Pract. 2016;35(2):96-101.   Published online February 27, 2016
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A Case of Familial Atypical Hemolytic Uremic Syndrome Associated with Complement Factor H Mutation in Adults
Hyun Kee Lee, M.D. Hee Kyung Na, M.D. Ji Young Lee, M.D. Jai Won Chang, M.D. Won Seok Yang, M.D. Soon Bae Kim, M.D. Jung Sik Park, M.D. Su Kil Park, M.D. Soon Kil Kwon, M.D. and Hae Il Cheong, M.D.
Korean J Nephrol. 2009;28(3):259-264.
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APCN_KSN_2024

Kidney Research
and
Clinical Practice

Print ISSN: 2211-9132
Online ISSN: 2211-9140



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