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Braunisch, M. et al. (2018). Extension of the phenotype of biallelic loss‐of‐function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I. Clinical genetics. 93 (2), pp. 255-265. [Online].
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Braunisch, M. et al. (2018). Extension of the phenotype of biallelic loss‐of‐function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I. Clinical genetics. 93 (2), pp. 255-265. [Online].