Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features

  1. Valdivielso-Ramos, M.
  2. Solera, J.
  3. Mauleon, C.
  4. Hernanz, J.M.
  5. Amiñoso, C.
  6. Galiano, S.
  7. De La Cueva, P.
Aldizkaria:
Clinical and Experimental Dermatology

ISSN: 1365-2230 0307-6938

Argitalpen urtea: 2014

Alea: 39

Zenbakia: 3

Orrialdeak: 406-407

Mota: Gutuna

DOI: 10.1111/CED.12291 GOOGLE SCHOLAR