Zobrazeno 1 - 1
of 1
pro vyhledávání: '"mutaciones anuladoras"'
Publikováno v:
Revista Finlay, Vol 12, Iss 4, Pp 491-495 (2022)
Baller-Gerold syndrome is secondary to mutations in the RECQL4 gene (8q24.3). This gene belongs to the RecQhelicase family and is implicated in other diseases predisposing to cancer. Diagnosis is based on clinical criteria and due to the high number
Externí odkaz:
https://doaj.org/article/9a8c1bbd180e422aa5a6855e1a057f4d
