A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary

Sümegi, AndreaHendrik, ZoltánGáll, TamásFelszeghy, Enikő NoémiSzakszon, KatalinAntal-Szalmás, PéterBeke, LíviaPapp, ÁgnesMéhes, GáborBalla, JózsefBalla, György2021-01-062021-01-062020BMC Medical Genetics. -21 : 61 (2020), p. 1-12. -BMC Med. Genet. - 1471-2350. - 1471-23501471-2350http://hdl.handle.net/2437/300850A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungaryidegen nyelvű folyóiratközlemény külföldi lapbanopen access journalhttp://webpac.lib.unideb.hu:8082/ebib/CorvinaWeb?action=cclfind&resultview=long&ccltext=idno+BIBFORM090236OrvostudományokKlinikai orvostudományokhttps://bmcmedgenet.biomedcentral.com/articles/10.1186/s12881-020-0985-6http://dx.doi.org/10.1186/s12881-020-0985-62021-03-27