Author: "Kocoglu, Cemile" / Publisher: ovid technologies (wolters kluwer health) - Searchworks@Jio Institute Digital Library Search Results

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Your search keyword '"Kocoglu, Cemile"' showing total 2 results

Start Over Author "Kocoglu, Cemile" Publisher ovid technologies (wolters kluwer health)

2 results on '"Kocoglu, Cemile"'

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

Author: Kocoglu, Cemile, primary, Gundogdu, Asli, additional, Kocaman, Gulsen, additional, Kahraman-Koytak, Pinar, additional, Uluc, Kayihan, additional, Kiziltan, Gunes, additional, Caglayan, Ahmet Okay, additional, Bilguvar, Kaya, additional, Vural, Atay, additional, and Basak, A. Nazli, additional
Published: 2018
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2. Turkish families with juvenile motor neuron disease broaden the phenotypic spectrum ofSPG11

Author: Iskender, Ceren, primary, Kartal, Ece, additional, Akcimen, Fulya, additional, Kocoglu, Cemile, additional, Ozoguz, Aslihan, additional, Kotan, Dilcan, additional, Eraksoy, Mefkure, additional, Parman, Yesim G., additional, and Basak, Ayse Nazli, additional
Published: 2015
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