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Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations.

Molecular genetics & genomic medicine - 1 Feb 2022

Ramsey Keri, Belnap Newell, Bonfitto Anna, Jepsen Wayne, Naymik Marcus, Sanchez-Castillo Meredith, Craig David W, Szelinger Szabolcs, Huentelman Matthew J, Narayanan Vinodh, Rangasamy Sampath

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PMID: 34994087
DOI: 10.1002/mgg3.1857
PMCID: PMC8830808

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