检索结果 - Fuat Aksu
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Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease 由 Birgit Uhlenberg, Markus Schuelke, Franz Rüschendorf, Nico Ruf, Angela M. Kaindl, Marco Henneke, Hölger Thiele, Gisela Stoltenburg‐Didinger, Fuat Aksu, Haluk Topaloğlu, Peter Nürnberg, Christoph Hübner, Bernhard Weschke, Jutta Gärtner
出版 2004Artigo -
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The Clinical Phenotype of Succinic Semialdehyde Dehydrogenase Deficiency (4-Hydroxybutyric Aciduria): Case Reports of 23 New Patients 由 K. Michael Gibson, Ernst Christensen, Cornelis Jakobs, Brian Fowler, Michael A. Clarke, G. Hammersen, K Raab, Joyce A. Kobori, Allie Moosa, Brigitte Vollmer, Eva Rossier, A. Kimberly Iafolla, Dietrich Matern, Oebele F. Brouwer, Janice E. Finkelstein, Fuat Aksu, H. P. WEBER, J. A. J. M. Bakkeren, F.J.M. Gabreëls, Daniel L. Bluestone, Todd F. Barron, Pierre Beauvais, Daniel Rabier, César Santos, Richard Umansky, W. Lehnert
出版 1997Artigo
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