Published in

Wiley, Movement Disorders, 2(32), p. 287-291, 2016

DOI: 10.1002/mds.26824

Links

Tools

Export citation

Search in Google Scholar

PTRHD1(C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism: PTRHD1Mutation In ID and Parkinsonism

Journal article published in 2016 by Hamidreza Khodadadi, Luis J. Azcona, Vajiheh Aghamollaii, Mir Davood Omrani, Masoud Garshasbi, Shaghayegh Taghavi, Abbas Tafakhori, Gholam Ali Shahidi, Javad Jamshidi ORCID, Hossein Darvish, Coro Paisán-Ruiz
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Red circle
Preprint: archiving forbidden
Red circle
Postprint: archiving forbidden
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO