Mutational and Phenotypic Spectra of KCNE1 deficiency in Jervell and Lange ‐Nielsen Syndrome and Romano‐Ward Syndrome

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Source: Human Mutation - November 21, 2018 Category: Genetics & Stem Cells Authors: Rabia Faridi, Risa Tona, Alessandra Brofferio, Michael Hoa, Rafal Olszewski, Isabelle Schrauwen, Muhammad Z.K. Assir, Akhtar A. Bandesha, Asma A. Khan, Atteeq U. Rehman, Carmen Brewer, Wasim Ahmed, Suzanne M. Leal, Sheikh Riazuddin, Steven E Tags: MUTATION UPDATE Source Type: research