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Ardalan-Shoja-Kiuru syndrome - Hereditary gelsolin amyloidosis plus retinitis pigmentosa

dc.contributor.authorShokouhi, G
dc.contributor.authorKhosroshahi, HT
dc.date.accessioned2018-08-26T08:35:18Z
dc.date.available2018-08-26T08:35:18Z
dc.date.issued2008
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52635
dc.description.abstract[No abstract available]
dc.language.isoEnglish
dc.relation.ispartofNephrology Dialysis Transplantation
dc.subjectgelsolin
dc.subjectgelsolin
dc.subjectamyloidosis
dc.subjectardalan shoja kiuru syndrome
dc.subjectautosomal dominant inheritance
dc.subjectchromosome 9q
dc.subjectcornea dystrophy
dc.subjectcutis laxa
dc.subjectfamily study
dc.subjectgene location
dc.subjectgene locus
dc.subjectgene mutation
dc.subjectgenetic disorder
dc.subjecthereditary gelsolin amyloidosis and retinitis pigmentosa
dc.subjecthuman
dc.subjectIran
dc.subjectIreland
dc.subjectletter
dc.subjectneuropathy
dc.subjectperception deafness
dc.subjectpriority journal
dc.subjectrare disease
dc.subjectretinitis pigmentosa
dc.subjectsyndrome
dc.subjectcongenital cornea dystrophy
dc.subjectcutis laxa
dc.subjectfamilial amyloidosis
dc.subjectgenetics
dc.subjectmutation
dc.subjectnote
dc.subjectretinitis pigmentosa
dc.subjectsyndrome
dc.subjectAmyloidosis, Familial
dc.subjectCorneal Dystrophies, Hereditary
dc.subjectCutis Laxa
dc.subjectGelsolin
dc.subjectHumans
dc.subjectMutation
dc.subjectRetinitis Pigmentosa
dc.subjectSyndrome
dc.titleArdalan-Shoja-Kiuru syndrome - Hereditary gelsolin amyloidosis plus retinitis pigmentosa
dc.typeArticle
dc.citation.volume23
dc.citation.issue3
dc.citation.spage1071
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1093/ndt/gfm577


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