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Paper Details

Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations.
Mol Genet Genomic Med
1
2022
Author NameAffiliation
David W CraigKeck School of Medicine, University of Southern California
Szabolcs SzelingerCenter for Rare Childhood Disorders, Translational Genomics Research Institute
Matthew J HuentelmanCenter for Rare Childhood Disorders, Translational Genomics Research Institute
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