Scotton, C., Italyankina, E., Storbeck, M., Vezyroglou, K., Heller, R., Neri, M., Di Raimo, F., Mauro, A., Tugnoli, V., Timmerman, V., Wirth, B., De Grandis, D., Gualandi, F. and Ferlini, A. (2015). Next generation sequencing identifies a novel ATP7A mutation in two brothers with distal hereditary motor neuropathy and autonomic dysfunction. Neuromusc. Disord., 25. S. S224 - 2. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364

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Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Scotton, C.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Italyankina, E.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Storbeck, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Vezyroglou, K.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Heller, R.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Neri, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Di Raimo, F.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mauro, A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Tugnoli, V.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Timmerman, V.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Wirth, B.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
De Grandis, D.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Gualandi, F.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Ferlini, A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-391302
DOI: 10.1016/j.nmd.2015.06.146
Journal or Publication Title: Neuromusc. Disord.
Volume: 25
Page Range: S. S224 - 2
Date: 2015
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
URI: http://kups.ub.uni-koeln.de/id/eprint/39130

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