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Author/Creator Halperin, Daniel

11. Nocturnal Atrial Fibrillation Caused by Mutation in KCND2, Encoding Pore-Forming (α) Subunit of the Cardiac Kv4.2 Potassium Channel. (November 2018)

Authors:
Drabkin, Max; Zilberberg, Noam; Menahem, Sasson; Mulla, Wesam; Halperin, Daniel; Yogev, Yuval; Wormser, Ohad; Perez, Yonatan; Kadir, Rotem; Etzion, Yoram; Katz, Amos; Birk, Ohad S.
Journal:
Circulation
Issue:
Volume 11:Number 11(2018)
Page Start:
Record Type:
Journal Article
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14. SEC31A mutation affects ER homeostasis, causing a neurological syndrome. Issue 3 (21st November 2018)

Authors:
Halperin, Daniel; Kadir, Rotem; Perez, Yonatan; Drabkin, Max; Yogev, Yuval; Wormser, Ohad; Berman, Erez M; Eremenko, Ekaterina; Rotblat, Barak; Shorer, Zamir; Gradstein, Libe; Shelef, Ilan; Birk, Ruth; Abdu, Uri; Flusser, Hagit; Birk, Ohad S
Journal:
Journal of medical genetics
Issue:
Volume 56:Issue 3(2019)
Page Start:
139
Record Type:
Journal Article
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