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Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations

Keri Ramsey1, Newell Belnap1, Anna Bonfitto1

  • 1Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, USA.

Molecular Genetics & Genomic Medicine
|January 7, 2022
PubMed
Summary

No abstract available in PubMed .

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