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Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency
Ben Yaou, Rabah, Hubert, Aurélie, Nelson, Isabelle, Dahlqvist, Julia R., Gaist, David, Streichenberger, Nathalie, Beuvin, Maud, Krahn, Martin, Petiot, Philippe, Parisot, Frédéric, Michel, Fabrice, MalVolume:
3
Journal:
Neurology Genetics
DOI:
10.1212/NXG.0000000000000208
Date:
December, 2017
File:
PDF, 622 KB
2017