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

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dc.contributor.authorsKocoglu, Cemile; Gundogdu, Asli; Kocaman, Gulsen; Kahraman-Koytak, Pinar; Uluc, Kayihan; Kiziltan, Gunes; Caglayan, Ahmet Okay; Bilguv, Kaya; Vural, Atay; Basak, A. Nazli
dc.date.accessioned2022-03-14T09:03:58Z
dc.date.accessioned2026-01-11T17:14:55Z
dc.date.available2022-03-14T09:03:58Z
dc.date.issued2018-02
dc.identifier.doi10.1212/NXG.0000000000000218
dc.identifier.issn2376-7839
dc.identifier.pubmed29379883
dc.identifier.urihttps://hdl.handle.net/11424/242347
dc.identifier.wosWOS:000430501700010
dc.language.isoeng
dc.publisherLIPPINCOTT WILLIAMS & WILKINS
dc.relation.ispartofNEUROLOGY-GENETICS
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleHomozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
dc.typearticle
dspace.entity.typePublication
oaire.citation.issue1
oaire.citation.titleNEUROLOGY-GENETICS
oaire.citation.volume4

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