A novel claudin-10 mutation with a unique mechanism in two unrelated families with HELIX syndrome Article

International Collaboration

cited authors

  • Alzahrani, Ali S.; Hussein, Maged; Alswailem, Meshael; Mouna, Ahmad; Albalawi, Lina; Moria, Yosra; Jabbar, Mai Abdel; Shi, Yufei; Guenzel, Dorothee; Dasouki, Majed

Publication Date

  • August 1, 2021

webpage

published in

category

keywords

  • CLDN10
  • HELIX syndrome
  • claudin-10
  • claudins
  • hypermagnesemia
  • hypohidrosis
  • hypokalemia
  • ichthyosis
  • tight junctions
  • xerostomia

start page

  • 415

end page

  • 429

volume

  • 100

issue

  • 2