Associated Papers
Genetic mutations in lymphocytic variant of hypereosinophilic syndrome: study of five siblings.
Walkenhorst M et al.
Frontiers in Medicine, 2025
41488087 (PubMed )
Supplement: Table_1.xlsx › Data
Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene.
Chen L et al.
Cell Death & Disease, 2020
Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance.
Nagara M et al.
European Journal of Medical Genetics, 2018
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss.
Stover EH et al.
Journal of Medical Genetics, 2002
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