MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases. (2021)
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.73907
Publication URI: https://www.repository.cam.ac.uk/handle/1810/326454
Type: Journal Article/Review