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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.64540

Publication URI: https://www.repository.cam.ac.uk/handle/1810/317427

Type: Journal Article/Review