Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion (2020)

First Author: McMacken G

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.60219

Publication URI: https://www.repository.cam.ac.uk/handle/1810/313116

Type: Other