検索結果 - M. Colak
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<scp>PLA2G6</scp> mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia 著者: 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
出版事項 2017Artigo