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Continue to ChatSNX14 Sorting Nexin 14 gene mutation causes a new syndromic form of cerebellar atrophy in a Turkish family - https://avesis.hacettepe.edu.tr/publication/details/473418aa-9f09-46d9-ba4b-dd7e202f8881/snx14-sorting-nexin-14-gene-mutation-causes-a-new-syndromic-form-of-cerebellar-atrophy-in-a-turkish-family