BASAL CELL NEVUS (GORLIN) SYNDROME WITH A NOVEL HETEROZYGOUS DELETION FRAMESHIFT MUTATION (C.959DELC, P.VAL322 PHE FSX2) IN THE PTCH1 GENE ASSOCIATED WITH EPIRETINAL MEMBRANE, ODONTOGENIC KERATOCYSTS AND WITHOUT SKIN LESIONS AND FALX CEREBRI CALCIFICATION

Akaltun, A.Eröz, RecepDoğan, MustafaBolu, SemihÖnder, Halil İbrahimOnbaş, O.Kocabay, Kenan2020-04-302020-04-3020161015-8146https://hdl.handle.net/20.500.12684/2894WOS: 000380178500017PubMed: 29485834…eninfo:eu-repo/semantics/closedAccessBASAL CELL NEVUS (GORLIN) SYNDROME WITH A NOVEL HETEROZYGOUS DELETION FRAMESHIFT MUTATION (C.959DELC, P.VAL322 PHE FSX2) IN THE PTCH1 GENE ASSOCIATED WITH EPIRETINAL MEMBRANE, ODONTOGENIC KERATOCYSTS AND WITHOUT SKIN LESIONS AND FALX CEREBRI CALCIFICATIONLetter272259262WOS:000380178500017N/AQ4