Ruling in a Suspect: The Role of AP2S1 Mutations in Familial Hypocalciuric Hypercalcemia Type 3

Ítems similars

• Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3
  per: Nesbit, M. Andrew, et al.
  Publicat: (2012)
• SAT-361 Familial Hypocalciuric Hypercalcemia Type 3: AP2S1 Mutation
  per: Kerut, Sarah Elizabeth, et al.
  Publicat: (2020)
• Clinical Presentation and Management Approach in a Case of Familial Hypocalciuric Hypercalcemia Type 3 Due to APS21 Gene Mutation
  per: Elsheikh, Sahar A, et al.
  Publicat: (2021)
• Familial hypocalciuric hypercalcaemia type 3: AP2S1 missense mutation
  per: Kerut, Sarah, et al.
  Publicat: (2020)
• Familial hypocalciuric hypercalcemia.
  per: Baxi, S C, et al.
  Publicat: (1982)