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Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations

Detalles Bibliográficos
Autores principales:	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
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8830808/ https://www.ncbi.nlm.nih.gov/pubmed/34994087 http://dx.doi.org/10.1002/mgg3.1857

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