Resultados da busca - M. Colak

<scp>PLA2G6</scp> mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia por 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