Associated Papers
A novel compound heterozygous mutation of the CLCN7 gene is associated with autosomal recessive osteopetrosis.
Wang X et al.
Frontiers in Pediatrics, 2023
CLCN7-related neuropathic infantile osteopetrosis in siblings.
Tachikawa J et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2021
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