Identification of c.104T>G, p.Met35Arg (NM_00314.8) heterozygous variant in exon 2 of PTEN as the causative factor for Cowden syndrome: a medical case study

  1. Mansilla-Polo, M.
  2. Escutia-Muñoz, B.
  3. Llavador-Ros, M.
  4. Botella-Estrada, R.
Aldizkaria:
Clinical and experimental dermatology

ISSN: 1365-2230

Argitalpen urtea: 2024

Alea: 49

Zenbakia: 2

Orrialdeak: 203-205

Mota: Artikulua

DOI: 10.1093/CED/LLAD344 GOOGLE SCHOLAR
Datuen iturria: Scopus