Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion (2020)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.17863/cam.73008
Publication URI: https://www.repository.cam.ac.uk/handle/1810/325551
Type: Other