Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Cemre Coşkun"'
Autor:
Mehmet Ali Akalin, Cemre Coşkun, Oznur Tastan, Tahsin Akgün, Ersin Tan, Aslihan Ozoguz Erimis, Mustafa Ertas, Halil Atilla Idrisoglu, Aysun Soysal, Erdi Şahin, Hamid Hamzeiy, Yesim Parman, Filiz Koç, Başar Bilgiç, Hasmet Hanagasi, Arman Çakar, Esra Gürsoy, Feza Deymeer, Ece Kartal, Fikret Aysal, Seyit Zor, Gulsen Babacan Yildiz, Nilda Turgut, Baris Isak, Gulden Olgun, Robin Palvadeau, Cemile Kocoglu, Fulya Akçimen, Tuncay Seker, Ersen Kavak, Elif Bayraktar, Utku Norman, A. Nazli Basak, A. Ercument Cicek, Ceren Tunca, Oguzhan Karakahya, Piraye Oflazer, Nesli-Ece Sen, Nurten Uzun Adatepe, Kayihan Uluc, Hacer Durmus, Cavit Boz, Dilcan Kotan
Publikováno v:
Human Mutation
Olgun, Gulden/0000-0002-4467-1610; Sahin, Erdi/0000-0002-5792-2888; Tastan, Oznur/0000-0001-7058-5372; Akcimen, Fulya/0000-0003-0931-5247; Kartal, Ece/0000-0002-7720-455X WOS:000542467300001 PubMed ID: 32579787 The last decade has proven that amyotro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54aef9b9d80c46be68614b3500ccd9db
http://hdl.handle.net/20.500.12645/18569
http://hdl.handle.net/20.500.12645/18569
Autor:
Ceren Tunca, Tuncay Şeker, Fulya Akçimen, Cemre Coşkun, Elif Bayraktar, Robin Palvadeau, Seyit Zor, Cemile Koçoğlu, Ece Kartal, Nesli Ece Şen, Hamid Hamzeiy, Aslıhan Özoğuz Erimiş, Utku Norman, Oğuzhan Karakahya, Gülden Olgun, Tahsin Akgün, Hacer Durmuş, Erdi Şahin, Arman Çakar, Esra Başar Gürsoy, Gülsen Babacan Yıldız, Barış İşak, Kayıhan Uluç, Haşmet Hanağası, Başar Bilgiç, Nilda Turgut, Fikret Aysal, Mustafa Ertaş, Cavit Boz, Dilcan Kotan, Halil İdrisoğlu, Aysun Soysal, Nurten Uzun Adatepe, Mehmet Ali Akalın, Filiz Koç, Ersin Tan, Piraye Oflazer, Feza Deymeer, Öznur Taştan, A. Ercüment Çiçek, Erşen Kavak, Yeşim Parman, A. Nazlı Başak
Publikováno v:
Human Mutation. 41
Autor:
Can Ebru Bekircan-Kurt, Betül Çevik, Cemile Kocoglu, Cemre Coşkun, Fulya Akçimen, A. Nazli Basak, Ersin Tan, Ceren Tunca, Aslı Gündoğdu-Eken
Publikováno v:
European Journal of Human Genetics. 26:745-748
WOS:000431829000017 PubMed: 29453415 Amyotrophic lateral sclerosis (ALS) is a late-onset motor neuron disease with mostly dominant inheritance and a life expectancy of 2-5 years; however, a quite common occurrence of atypical forms of the disease, du