Resultats de la cerca - Beyza Ciftci-Kavaklioglu
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<scp>PLA2G6</scp> mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia per Burçak Özeş, N. Karagoz, Rebecca Schüle, Adriana Rebelo, María‐Jesús Sobrido, Florian Harmuth, Matthis Synofzik, Samuel Ignacio Pascual Pascual, M. Colak, Beyza Ciftci-Kavaklioglu, Bülent Kara, Andrés Ordóñez‐Ugalde, Beatriz Quintáns, Michael Gonzalez, Aysun Soysal, Stephan Züchner, Esra Battaloğlu
Publicat 2017Artigo