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BETA-THALASSEMIA IN IRAN - A HIGH-INCIDENCE OF THE NONSENSE CODON-39 MUTATION ON THE ISLAND OF QUESHM

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dc.contributor.authorsNOORIDALOII, MR; MOAZAMI, N; FARHANGI, S; ATALAY, A; GEREN, IN; AKAR, L; ATALAY, EO; CIRAKOGLU, B; BERMEK, E
dc.date.accessioned2022-03-13T23:23:21Z
dc.date.accessioned2026-01-10T17:41:59Z
dc.date.available2022-03-13T23:23:21Z
dc.date.issued1994
dc.identifier.doi10.3109/03630269409045779
dc.identifier.issn0363-0269
dc.identifier.pubmed7713751
dc.identifier.urihttps://hdl.handle.net/11424/238537
dc.identifier.wosWOS:A1994PY45300011
dc.language.isoeng
dc.publisherINFORMA HEALTHCARE
dc.relation.ispartofHEMOGLOBIN
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPRENATAL-DIAGNOSIS
dc.subjectMOLECULAR-BASIS
dc.subjectTURKEY
dc.subjectSPECTRUM
dc.subjectGENES
dc.titleBETA-THALASSEMIA IN IRAN - A HIGH-INCIDENCE OF THE NONSENSE CODON-39 MUTATION ON THE ISLAND OF QUESHM
dc.typeother
dc.type.subnote
dspace.entity.typePublication
oaire.citation.endPage453
oaire.citation.issue6
oaire.citation.startPage449
oaire.citation.titleHEMOGLOBIN
oaire.citation.volume18

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