Karakaya, M., Kunde, V., Heller, R., Nuernberg, P. and Cirak, S. (2015). WES revealed a de-novo missense mutation in the NALCN gene in a Freeman-Sheldon-(DA2A) like syndrome with CNS involvement. Neuromusc. Disord., 25. S. S277 - 1. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 1873-2364

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Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Karakaya, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kunde, V.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Heller, R.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nuernberg, P.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Cirak, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-391294
DOI: 10.1016/j.nmd.2015.06.328
Journal or Publication Title: Neuromusc. Disord.
Volume: 25
Page Range: S. S277 - 1
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/39129

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