Published in
Elsevier, Genetics in Medicine, 10(25), p. 100961, 2023
DOI: 10.1016/j.gim.2023.100961
Elsevier, Genetics in Medicine, 10(24), p. 2079-2090, 2022
DOI: 10.1016/j.gim.2022.07.006
Links
Tools
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy
Journal article published in 2022 by
Joohyun Park 
,
Arianna Tucci,
Valentina Cipriani,
German Demidov,
Clarissa Rocca,
Jan Senderek,
Michaela Butryn,
Ana Velic,
Tanya Lam,
Evangelia Galanaki,
Elisa Cali,
Letizia Vestito,
Reza Maroofian,
Natalie Deininger,
Maren Rautenberg
and other authors.
,
Arianna Tucci,
Valentina Cipriani,
German Demidov,
Clarissa Rocca,
Jan Senderek,
Michaela Butryn,
Ana Velic,
Tanya Lam,
Evangelia Galanaki,
Elisa Cali,
Letizia Vestito,
Reza Maroofian,
Natalie Deininger,
Maren Rautenberg
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Postprint:
archiving forbidden
Published version:
archiving forbidden
Data provided by 