Search Results - Hadas Lahat
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1
A Missense Mutation in the LIM2 Gene Is Associated with Autosomal Recessive Presenile Cataract in an Inbred Iraqi Jewish Family by Eran Pras, Etgar Levy‐Nissenbaum, Tangiz Bakhan, Hadas Lahat, Ehud I. Assia, Noa Geffen-Carmi, Moshe Frydman, Boleslaw Goldman, Elon Pras
Published 2002Artigo -
2
Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia by Hadas Lahat, Michael Eldar, Etgar Levy‐Nissenbaum, Tangiz Bahan, Eitan Friedman, Asad Khoury, Avraham Lorber, Daniel L. Kastner, Boleslaw Goldman, Elon Pras
Published 2001Artigo -
3
A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from... by Hadas Lahat, Elon Pras, Tsviya Olender, Nili Avidan, Edna Ben‐Asher, Orna Man, Etgar Levy‐Nissenbaum, Asad Khoury, Avraham Lorber, Boleslaw Goldman, Doron Lancet, Michael Eldar
Published 2001Artigo
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Biology
Gene
Genetics
Catecholaminergic polymorphic ventricular tachycardia
Internal medicine
Medicine
Missense mutation
Mutation
Ryanodine receptor
Ryanodine receptor 2
Asymptomatic
Blood pressure
Bradycardia
Calcium
Cardiology
Cataracts
Catecholamine
Chromosome
Developmental psychology
Heart rate
Locus (genetics)
Penetrance
Phenotype
Psychology
Receptor
Sibling
Sinus bradycardia
Sudden death
Tachycardia
Ventricular tachycardia