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STXBP1 Stop‐Loss Mutation Associated with Complex Early Onset Movement Disorder without Epilepsy

Detalles Bibliográficos
Autores principales:	Spaull, Robert, Steel, Dora, Barwick, Katy, Prabhakar, Prab, Wakeling, Emma, Kurian, Manju A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2022
Materias:	Letters: Genotype and Phenotype
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346254/ https://www.ncbi.nlm.nih.gov/pubmed/35937496 http://dx.doi.org/10.1002/mdc3.13509

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