An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.

Ítems similars

• X-linked recessive hypoparathyroidism is caused by a molecular deletional-insertion involving chromosomes Xq27 and 2p25.
  per: Bowl, MR, et al.
  Publicat: (2001)
• X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase.
  per: Andrew Nesbit, M, et al.
  Publicat: (2004)
• Studies of mice deleted for Sox3 and uc482: Relevance to X-linked hypoparathyroidism
  per: Gaynor, KU, et al.
  Publicat: (2020)
• Genetic mapping studies of the X-linked recessive hypoparathyroid gene on the X chromosome (Xq27).
  per: Dixon, P, et al.
  Publicat: (1996)
• Physical map of the Xq27 candidate region for X-linked recessive hypoparathyroidism in two kindreds merged by mitochondrial DNA analysis
  per: Mumm, S, et al.
  Publicat: (1996)