Mutations in POGLUT1 in Galli–Galli/Dowling–Degos disease

Ítems similars

• Galli-Galli Disease: A Rare Acantholytic Variant of Dowling-Degos Disease
  per: Gomes, J., et al.
  Publicat: (2011)
• Hidradenitis Suppurativa Associated with Galli-Galli Disease: Extending the Link with Dowling-Degos Disease
  per: Del Mar, María, et al.
  Publicat: (2020)
• Heterozygous frameshift mutation in keratin 5 in a family with Galli–Galli disease
  per: Reisenauer, AK, et al.
  Publicat: (2014)
• Altered Notch signaling in Dowling-Degos disease: Additional mutations in POGLUT1 and further insights into disease pathogenesis
  per: Ralser, Damian J., et al.
  Publicat: (2018)
• Mutations in POGLUT1, Encoding Protein O-Glucosyltransferase 1, Cause Autosomal-Dominant Dowling-Degos Disease
  per: Basmanav, F. Buket, et al.
  Publicat: (2014)