A unique triadin exon deletion causing a null phenotype

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Bibliographic Details
Published inHeartRhythm case reports Vol. 4; no. 11; pp. 514 - 518
Main Authors 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
Format Report
LanguageEnglish
Published 01.11.2018
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Bibliography:ObjectType-Case Study-2
content type line 59
SourceType-Reports-1
ObjectType-Report-1
ISSN:2214-0271
2214-0271
DOI:10.1016/j.hrcr.2018.07.014