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1

Molecular diagnosis of solute carrier family 4 member 1 (SLC4A1) mutation-related autosomal recessive distal renaltubular acidosis

Molecular diagnosis of solute carrier family 4 member 1 (SLC4A1) mutation-related autosomal recessive distal renaltubular acidosis

بواسطة Nipaporn Deejai, Suwannee Wisanuyotin, Choochai Nettuwakul, Sookkasem Khositseth, Nunghathai Sawasdee, Kiattichai Saetai, Pathai Yenchitsomanus, Nanyawan Rungroj
منشور في 2020

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2

A novel loss-of-function mutation of PBK associated with human kidney stone disease

A novel loss-of-function mutation of PBK associated with human kidney stone disease

بواسطة Choochai Nettuwakul, Nunghathai Sawasdee, Oranud Praditsap, Nanyawan Rungroj, Arnat Pasena, Thanyaporn Dechtawewat, Nipaporn Deejai, Suchai Sritippayawan, Santi Rojsatapong, Wipada Chaowagul, Pa thai Yenchitsomanus
منشور في 2020

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