Neurological involvement in Glycogen Storage Disease type IXa due to PHKA2 mutation.

Neurological involvement in Glycogen Storage Disease type IXa due to PHKA2 mutation. Can J Neurol Sci. 2020 Jan 28;:1-13 Authors: Smith C, Care4Rare Canada Consortium, Dicaire MJ, Brais B, Piana R PMID: 31987065 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/31987065?dopt=Abstract

Source: The Canadian Journal of Neurological Sciences - January 27, 2020 Category: Neurology Authors: Smith C, Care4Rare Canada Consortium, Dicaire MJ, Brais B, Piana R Tags: Can J Neurol Sci Source Type: research

More News: Brain | Canada Health | Neurology