Delle Vedove, A., Zanni, G., Eckenweiler, M., Storbeck, M., Barresi, S., Pizzi, S., Hosseinibarkooie, S., Mendoza-Ferreira, N., Hoelker, I., Koerber, F., Kye, M., Bertini, E., Kirschner, J., Tartaglia, M. and Wirth, B. (2020). A recurrent de novo CAPRIN1 mutation causes a novel progressive early onset neurodegenerative disorder. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 404 - 405. LONDON: SPRINGERNATURE. ISSN 1476-5438

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Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Delle Vedove, A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Zanni, G.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Eckenweiler, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Storbeck, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Barresi, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Pizzi, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hosseinibarkooie, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mendoza-Ferreira, N.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hoelker, I.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Koerber, F.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kye, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Bertini, E.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kirschner, J.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Tartaglia, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Wirth, B.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-309071
Journal or Publication Title: Eur. J. Hum. Genet.
Volume: 28
Number: SUPPL 1
Page Range: S. 404 - 405
Date: 2020
Publisher: SPRINGERNATURE
Place of Publication: LONDON
ISSN: 1476-5438
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
Biochemistry & Molecular Biology; Genetics & HeredityMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/30907

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