Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/7144
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kaçar, N. | - |
dc.contributor.author | Semerci, N. | - |
dc.contributor.author | Ergin, Ş. | - |
dc.contributor.author | Pascucci, M. | - |
dc.contributor.author | Zambruno, G. | - |
dc.contributor.author | Castiglia, D. | - |
dc.date.accessioned | 2019-08-16T12:16:32Z | - |
dc.date.available | 2019-08-16T12:16:32Z | - |
dc.date.issued | 2008 | - |
dc.identifier.issn | 0007-0963 | - |
dc.identifier.uri | https://hdl.handle.net/11499/7144 | - |
dc.identifier.uri | https://doi.org/10.1111/j.1365-2133.2008.08553.x | - |
dc.description.abstract | Abstract Not Available | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | British Journal of Dermatology | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | KIND1 | en_US |
dc.subject | Kindler syndrome | en_US |
dc.subject | Mutation database | en_US |
dc.subject | Poikiloderma | en_US |
dc.subject | adolescent | en_US |
dc.subject | autosomal recessive disorder | en_US |
dc.subject | blood sampling | en_US |
dc.subject | case report | en_US |
dc.subject | clinical feature | en_US |
dc.subject | DNA sequence | en_US |
dc.subject | female | en_US |
dc.subject | frameshift mutation | en_US |
dc.subject | gene | en_US |
dc.subject | genodermatosis | en_US |
dc.subject | human | en_US |
dc.subject | human tissue | en_US |
dc.subject | kind1 gene | en_US |
dc.subject | kindler syndrome | en_US |
dc.subject | letter | en_US |
dc.subject | nucleotide sequence | en_US |
dc.subject | physical examination | en_US |
dc.subject | priority journal | en_US |
dc.subject | sibling | en_US |
dc.subject | skin biopsy | en_US |
dc.subject | Turkey (republic) | en_US |
dc.subject | Adolescent | en_US |
dc.subject | Blister | en_US |
dc.subject | DNA Mutational Analysis | en_US |
dc.subject | Female | en_US |
dc.subject | Frameshift Mutation | en_US |
dc.subject | Humans | en_US |
dc.subject | Membrane Proteins | en_US |
dc.subject | Neoplasm Proteins | en_US |
dc.subject | Pedigree | en_US |
dc.subject | Phenotype | en_US |
dc.subject | Photosensitivity Disorders | en_US |
dc.subject | Siblings | en_US |
dc.subject | Skin Diseases, Genetic | en_US |
dc.subject | Syndrome | en_US |
dc.subject | Turkey | en_US |
dc.title | A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome | en_US |
dc.type | Letter | en_US |
dc.identifier.volume | 158 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.startpage | 1375 | - |
dc.identifier.startpage | 1375 | en_US |
dc.identifier.endpage | 1377 | en_US |
dc.identifier.doi | 10.1111/j.1365-2133.2008.08553.x | - |
dc.relation.publicationcategory | Diğer | en_US |
dc.identifier.pmid | 18410424 | en_US |
dc.identifier.scopus | 2-s2.0-43749110671 | en_US |
dc.identifier.wos | WOS:000255960300031 | en_US |
dc.identifier.scopusquality | Q1 | - |
dc.owner | Pamukkale University | - |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Letter | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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