Identification of Two Novel Mutations of ABCD1 Gene in Pedigrees with X-Linked Adrenoleukodystrophy and Review of the LiteratureBingzi Dong, Yangang Wang, Xiaofang Sun et al.|International Journal of Endocrinology|2022Cited by 14
Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypesBingzi Dong, Wenjuan Zhao, Ying Chen et al.|BMC Nephrology|2020Cited by 9
Identification of two novel mutations of ABCD1 gene in pedigrees with X‐linked adrenoleukodystrophyBingzi Dong, Yangang Wang, Wenshan Lv et al.|Research Square|2020Cited by 1
Identification of Two Novel Mutations of ABCD1 Gene in Pedigrees With X‐linked Adrenoleukodystrophy and Review of the LiteraturesBingzi Dong, Yangang Wang, Wenshan Lv et al.|Research Square|2021Cited by 0
Identification of novel compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman's syndrome exhibiting Bartter's syndrome-liked phenotypesBingzi Dong, Wenjuan Zhao, Yuhang Zhao et al.|Research Square|2020Cited by 0