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Comment on “A New Allelic Variant in the PANK2 Gene in a Patient with Incomplete HARP Syndrome”

Detalles Bibliográficos
Autores principales:	Walker, Ruth Helen, Hegele, Robert Alexander, Danek, Adrian
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Movement Disorder Society 2021
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8490183/ https://www.ncbi.nlm.nih.gov/pubmed/33819419 http://dx.doi.org/10.14802/jmd.20145

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