Universität zu Köln

Petry-Schmelzer, Jan Niklas ORCID: 0000-0003-0749-3840, Keller, Natalie, Karakaya, Mert, Wirth, Brunhilde ORCID: 0000-0003-4051-5191, Fink, Gereon R. ORCID: 0000-0002-8230-1856 and Wunderlich, Gilbert (2021). VPS13D: One Family, Same Mutations, Two Phenotypes. MOV. DISORD. CLIN. PRACT., 8 (5). S. 803 - 807. HOBOKEN: WILEY. ISSN 2330-1619

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Item Type:	Journal Article
Creators:	Creators Email ORCID ORCID Put Code Petry-Schmelzer, Jan Niklas UNSPECIFIED orcid.org/0000-0003-0749-3840 UNSPECIFIED Keller, Natalie UNSPECIFIED UNSPECIFIED UNSPECIFIED Karakaya, Mert UNSPECIFIED UNSPECIFIED UNSPECIFIED Wirth, Brunhilde UNSPECIFIED orcid.org/0000-0003-4051-5191 UNSPECIFIED Fink, Gereon R. UNSPECIFIED orcid.org/0000-0002-8230-1856 UNSPECIFIED Wunderlich, Gilbert UNSPECIFIED UNSPECIFIED UNSPECIFIED
URN:	urn:nbn:de:hbz:38-577402
DOI:	10.1002/mdc3.13232
Journal or Publication Title:	MOV. DISORD. CLIN. PRACT.
Volume:	8
Number:	5
Page Range:	S. 803 - 807
Date:	2021
Publisher:	WILEY
Place of Publication:	HOBOKEN
ISSN:	2330-1619
Language:	English
Faculty:	Unspecified
Divisions:	Unspecified
Subjects:	no entry
Uncontrolled Keywords:	Keywords Language Clinical Neurology Multiple languages
URI:	http://kups.ub.uni-koeln.de/id/eprint/57740