Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant. (2020)
Attributed to:
New genomic approaches to explore the neurogenetic disease burden of consanguineous marriages in Turkey
funded by
Newton Fund
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.17863/cam.44915
Publication URI: https://www.repository.cam.ac.uk/handle/1810/297858
Type: Journal Article/Review