Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4

Abstract Background Coffin–Siris syndrome (CSS) is characterized by intellectual disability, dysmorphic facial features, growth deficiency, microcephaly, and abnormalities of the fifth fingers/toes. CSS is caused by mutations in several genes of the BRG1‐associated factor pathway including SMARCA4....

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Κύριοι συγγραφείς:	Gerarda Cappuccio, Raffaella Brunetti‐Pierri, Annalaura Torella, Michele Pinelli, Raffaele Castello, Giorgio Casari, Vincenzo Nigro, Sandro Banfi, Francesca Simonelli, TUDP, Nicola Brunetti‐Pierri
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	Wiley 2019-06-01
Σειρά:	Molecular Genetics & Genomic Medicine
Θέματα:	Coffin–Siris syndrome retinitis pigmentosa SMARCA4
Διαθέσιμο Online:	https://doi.org/10.1002/mgg3.682
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