Associated Papers
Late-Onset Bartter Syndrome Type II Due to a Novel Compound Heterozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review.
Tian M et al.
Frontiers in Medicine, 2022
Expanding the spectrum of genetic mutations in antenatal Bartter syndrome type II.
Fretzayas A et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2013
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