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Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families

dc.contributor.authorBilguv, Kaya
dc.contributor.authorKocoglu, Cemile
dc.contributor.authorGundogdu, Asli
dc.contributor.authorKAHRAMAN KOYTAK, PINAR
dc.contributor.authorULUÇ, KAYIHAN
dc.contributor.authorCaglayan, Ahmet Okay
dc.contributor.authorKocaman, Gulsen
dc.contributor.authorKiziltan, Gunes
dc.contributor.authorBasak, A. Nazli
dc.contributor.authorVural, Atay
dc.date.accessioned2021-03-05T17:53:52Z
dc.date.available2021-03-05T17:53:52Z
dc.date.issued2018
dc.identifier.citationKocoglu C., Gundogdu A., Kocaman G., KAHRAMAN KOYTAK P., ULUÇ K., Kiziltan G., Caglayan A. O. , Bilguv K., Vural A., Basak A. N. , "Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families", NEUROLOGY-GENETICS, cilt.4, 2018
dc.identifier.issn2376-7839
dc.identifier.otherav_c7c1d821-5eba-4445-a8da-44b81859b1fd
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/132395
dc.identifier.urihttps://doi.org/10.1212/nxg.0000000000000218
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.titleHomozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
dc.typeMakale
dc.relation.journalNEUROLOGY-GENETICS
dc.contributor.departmentBoğaziçi Üniversitesi , ,
dc.identifier.volume4
dc.identifier.issue1
dc.contributor.firstauthorID251455


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