Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Tarun Kumar Girigiri"'
Publikováno v:
Indian Pediatrics Case Reports, Vol 1, Iss 4, Pp 244-246 (2021)
Background: Raine syndrome is a rare autosomal recessive neonatal osteosclerotic bone dysplasia caused due to mutations in the FAM20C gene. It has an early and aggressive onset which often results in death in the first few weeks of life, although the
Externí odkaz:
https://doaj.org/article/44e1b89167c846ce83dd61d685a18598
