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

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Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Bayram, A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Stumpfe, K.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Wang, H.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Pergande, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Per, H.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Cirak, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-215809
DOI: 10.1016/j.nmd.2017.06.197
Journal or Publication Title: Neuromusc. Disord.
Volume: 27
Page Range: S. S147 - 1
Date: 2017
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Place of Publication: OXFORD
ISSN: 1873-2364
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
Clinical Neurology; NeurosciencesMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/21580

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