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PO-05-102 A NOVEL SLC4A3 MUTATION CAUSES SHORT QT SYNDROME: FROM MOLECULAR ANALYSIS TO PHENOTYPIC EXPRESSION AND NOVEL DIAGNOSTIC TESTING |
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Titel: |
PO-05-102 A NOVEL SLC4A3 MUTATION CAUSES SHORT QT SYNDROME: FROM MOLECULAR ANALYSIS TO PHENOTYPIC EXPRESSION AND NOVEL DIAGNOSTIC TESTING |
Auteur: |
Giladi, Moshe Chorin, Odelia Piccirillo, Silvia Prass, Elon Wolf, Haike Reznik Shamash, Jana Barel, Ortal Viskin, Dana Frydman, Shir Rosso, Raphael Banai, Shmuel Viskin, Sami Chorin, Ehud |
Verschenen in: |
Heart rhythm |
Paginering: |
Jaargang 22 () nr. 4S pagina's S609 |
Jaar: |
2025 |
Inhoud: |
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Uitgever: |
Published by Elsevier B.V. |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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