A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis. (2021)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.17863/cam.75938

Publication URI: https://www.repository.cam.ac.uk/handle/1810/328490

Type: Journal Article/Review