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Jump to: 2017 | 2016
Number of items: 2.

2017

Bayram, A., Stumpfe, K., Wang, H., Pergande, M., Per, H. and Cirak, S. (2017). Severe form of recessive Charcot-Marie-Tooth disease with a novel mutation in myotubularin related protein 2. Neuromusc. Disord., 27. S. S147 - 1. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364

2016

Bayram, A. Kacar, Per, H., Zorludemir, S., Wang, H., Gumus, H. and Cirak, S. (2016). A new homozygous frameshifting mutation in SPEG causes mild centronuclear myopathy. Neuromusc. Disord., 26. S. S117 - 2. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364

This list was generated on Sun May 5 05:11:11 2024 CEST.