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Presenting Features, Clinical Characteristics and Follow Up of Familial Isolated Glucocorticoid Deficiency (FGD) Due to Mutations in MC2R and MRAP Genes

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dc.contributor.authorsOzbek, Mehmet Nuri; Karasin, Nezehat Dogan; Demirbilek, Huseyin; Demiral, Meliha; Baran, Riza Taner; Guran, Tulay
dc.date.accessioned2022-03-10T17:57:51Z
dc.date.accessioned2026-01-11T06:06:30Z
dc.date.available2022-03-10T17:57:51Z
dc.date.issued2018
dc.identifier.doidoiWOS:000445204101082
dc.identifier.eissn1663-2826
dc.identifier.issn1663-2818
dc.identifier.urihttps://hdl.handle.net/11424/222110
dc.identifier.wosWOS:000445204101082
dc.language.isoeng
dc.publisherKARGER
dc.relation.ispartofHORMONE RESEARCH IN PAEDIATRICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titlePresenting Features, Clinical Characteristics and Follow Up of Familial Isolated Glucocorticoid Deficiency (FGD) Due to Mutations in MC2R and MRAP Genes
dc.typeconferenceObject
dc.type.submeetingabstract
dspace.entity.typePublication
oaire.citation.endPage162
oaire.citation.startPage161
oaire.citation.titleHORMONE RESEARCH IN PAEDIATRICS
oaire.citation.volume90

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