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dc.contributor.authorJordanova, Albena
dc.contributor.authorDurmuş, Hacer
dc.contributor.authorYapıcı, Zuhal
dc.contributor.authorParman, Yeşim
dc.contributor.authorBattaloğlu, Esra
dc.contributor.authorCandayan, Ayşe
dc.contributor.authorÇakar, Arman
dc.contributor.authorYunisova, Gulshan
dc.contributor.authorÖzdağ Acarlı, Ayşe Nur
dc.contributor.authorAtkinson, Derek
dc.contributor.authorTopaloğlu, Pınar
dc.date.accessioned2021-12-10T10:37:51Z
dc.date.available2021-12-10T10:37:51Z
dc.date.issued2021
dc.identifier.citationCandayan A., Çakar A., Yunisova G., Özdağ Acarlı A. N. , Atkinson D., Topaloğlu P., Durmuş H., Yapıcı Z., Jordanova A., Parman Y., et al., "Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort.", Neurology. Genetics, cilt.7, sa.5, 2021
dc.identifier.issn2376-7839
dc.identifier.othervv_1032021
dc.identifier.otherav_4adedfd3-f384-409b-adf8-0bc46c7e364c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/170278
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/4adedfd3-f384-409b-adf8-0bc46c7e364c/file
dc.identifier.urihttps://doi.org/10.1212/nxg.0000000000000621
dc.description.abstractBackground and Objectives Inherited peripheral neuropathies (IPNs) are a group of genetic disorders of the peripheral nervous system in which neuropathy is the only or the most predominant clinical feature. The most common type of IPN is Charcot-Marie-Tooth (CMT) disease. Autosomal recessive CMT (ARCMT) is generally more severe than dominant CMT and its genetic basis is poorly understood due to high clinical and genetic diversity. Here, we report clinical and genetic findings from 56 consanguineous Turkish families initially diagnosed with CMT disease.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.titleGenetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort.
dc.typeMakale
dc.relation.journalNeurology. Genetics
dc.contributor.department, ,
dc.identifier.volume7
dc.identifier.issue5
dc.contributor.firstauthorID2750502


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