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A unique triadin exon deletion causing a null phenotype

Detalles Bibliográficos
Autores principales:	O’Callaghan, Barry M., Hancox, Jules C., Stuart, Alan G., Armstrong, Catherine, Williams, Maggie M., Hills, Alison, Pearce, Hazel, Dent, Carolyn L., Gable, Mary, Walsh, Mark A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2018
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6241331/ https://www.ncbi.nlm.nih.gov/pubmed/30479949 http://dx.doi.org/10.1016/j.hrcr.2018.07.014

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