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Items where Author is "Anwar, N."

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Article

Wiessner, M. and Maroofian, R. and Ni, M.-Y. and Pedroni, A. and Müller, J.S. and Stucka, R. and Beetz, C. and Efthymiou, S. and Santorelli, F.M. and Alfares, A.A. and Zhu, C. and Uhrova Meszarosova, A. and Alehabib, E. and Bakhtiari, S. and Janecke, A.R. and Otero, M.G. and Chen, J.Y.H. and Peterson, J.T. and Strom, T.M. and De Jonghe, P. and Deconinck, T. and De Ridder, W. and De Winter, J. and Pasquariello, R. and Ricca, I. and Alfadhel, M. and Van De Warrenburg, B.P. and Portier, R. and Bergmann, C. and Ghasemi Firouzabadi, S. and Jin, S.C. and Bilguvar, K. and Hamed, S. and Abdelhameed, M. and Haridy, N.A. and Maqbool, S. and Rahman, F. and Anwar, N. and Carmichael, J. and Pagnamenta, A. and Wood, N.W. and Tran Mau-Them, F. and Haack, T. and Di Rocco, M. and Ceccherini, I. and Iacomino, M. and Zara, F. and Salpietro, V. and Scala, M. and Rusmini, M. and Xu, Y. and Wang, Y. and Suzuki, Y. and Koh, K. and Nan, H. and Ishiura, H. and Tsuji, S. and Lambert, L. and Schmitt, E. and Lacaze, E. and Küpper, H. and Dredge, D. and Skraban, C. and Goldstein, A. and Willis, M.J.H. and Grand, K. and Graham, J.M. and Lewis, R.A. and Millan, F. and Duman, �. and Dündar, N. and Uyanik, G. and Schöls, L. and Nürnberg, P. and Nürnberg, G. and Catala Bordes, A. and Seeman, P. and Kuchar, M. and Darvish, H. and Rebelo, A. and Bouçanova, F. and Medard, J.-J. and Chrast, R. and Auer-Grumbach, M. and Alkuraya, F.S. and Shamseldin, H. and Al Tala, S. and Rezazadeh Varaghchi, J. and Najafi, M. and Deschner, S. and Gläser, D. and Hüttel, W. and Kruer, M.C. and Kamsteeg, E.-J. and Takiyama, Y. and Züchner, S. and Baets, J. and Synofzik, M. and Schüle, R. and Horvath, R. and Houlden, H. and Bartesaghi, L. and Lee, H.-J. and Ampatzis, K. and Pierson, T.M. and Senderek, J. and Genomics England Research Consortium, PREPARE network (2021) Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. Brain, 144 (5). pp. 1422-1434.

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