Clinical and molecular characteristics of congenital hypothyroidism with DUOX2 mutations

Ítems similars

• Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism
  per: Aycan, Zehra, et al.
  Publicat: (2017)
• DUOX2 Mutations Are Frequently Associated With Congenital Hypothyroidism in the Korean Population
  per: Park, Kyoung-Jin, et al.
  Publicat: (2016)
• A family with Townes-Brocks syndrome with congenital hypothyroidism and a novel mutation of the SALL1 gene
  per: Choi, Won Ik, et al.
  Publicat: (2010)
• Zebrafish duox mutations provide a model for human congenital hypothyroidism
  per: Chopra, Kunal, et al.
  Publicat: (2019)
• Clinical course and endocrinological characteristics of prolactinoma in children and adolescents
  per: Kim, Yoo-Mi, et al.
  Publicat: (2013)