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

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dc.contributor.authorKocoglu, Cemile
dc.contributor.authorGundogdu, Asli
dc.contributor.authorKocaman, Gulsen
dc.contributor.authorKAHRAMAN KOYTAK, PINAR
dc.contributor.authorULUÇ, KAYIHAN
dc.contributor.authorKiziltan, Gunes
dc.contributor.authorCaglayan, Ahmet Okay
dc.contributor.authorBilguv, Kaya
dc.contributor.authorVural, Atay
dc.contributor.authorBasak, A. Nazli
dc.date.accessioned2020-10-22T19:36:26Z
dc.date.available2020-10-22T19:36:26Z
dc.date.issued2018-02-01T00:00:00Z
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.doi10.1212/nxg.0000000000000218
dc.identifier.pubmed29379883
dc.identifier.scopus85048716971
dc.identifier.urihttp://hdl.handle.net/20.500.12645/24571
dc.identifier.wosWOS:000430501700010
dc.titleHomozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
dc.typeArticle
dspace.entity.typePublication
local.avesis.idc7c1d821-5eba-4445-a8da-44b81859b1fd
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus
local.publication.isinternational1

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