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An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome

✍ Scribed by Zahurul A. Bhuiyan; Tarek S. Momenah; Ahmad S. Amin; Ayman S. Al-Khadra; Marielle Alders; Arthur A.M. Wilde; Marcel M.A.M. Mannens

Book ID: 113843493
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 624 KB
Volume: 98
Category: Article
ISSN: 0079-6107
DOI: 10.1016/j.pbiomolbio.2008.10.004

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