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Molecular Genetics & Genomic Medicine
(Feb 2022)
Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations
Keri Ramsey,
Newell Belnap,
Anna Bonfitto,
Wayne Jepsen,
Marcus Naymik,
Meredith Sanchez‐Castillo,
David W. Craig,
Szabolcs Szelinger,
Matthew J. Huentelman,
Vinodh Narayanan,
Sampath Rangasamy
Affiliations
Keri Ramsey
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
Newell Belnap
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
Anna Bonfitto
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
Wayne Jepsen
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
Marcus Naymik
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
Meredith Sanchez‐Castillo
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
David W. Craig
Department of Translational Genomics Keck School of Medicine University of Southern California Los Angeles California USA
Szabolcs Szelinger
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
Matthew J. Huentelman
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
Vinodh Narayanan
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
Sampath Rangasamy
Center for Rare Childhood Disorders Translational Genomics Research Institute Phoenix Arizona USA
DOI
https://doi.org/10.1002/mgg3.1857
Journal volume & issue
Vol. 10, no. 2
pp. n/a – n/a
Abstract
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No abstracts available.
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