Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

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Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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2017年论文

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2017年论文

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Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

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Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

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Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

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P1476

Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia

@en

P2093

Amnah Y Bdier

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Arthur A M Wilde

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Bandar Alshehri

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Jumana Y Al-Aama

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Khalid Dagriri

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Omamah A Jiman

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Saleh Al-Ghamdi

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Sherif E Ahmed

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P2860

Familial sinus bradycardia associated with a mutation in the cardiac pacemaker channel

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

Novel compound heterozygous mutations in the KCNQ1 gene associated with autosomal recessive long QT syndrome (Jervell and Lange-Nielsen syndrome).

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.

The homozygous KCNQ1 gene mutation associated with recessive Romano-Ward syndrome.

The long QT syndrome. Prospective longitudinal study of 328 families.

Long QT syndrome in South Africa: the results of comprehensive genetic screening.

Genetic and clinical advances in congenital long QT syndrome.

Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.

Prevalence and potential genetic determinants of sensorineural deafness in KCNQ1 homozygosity and compound heterozygosity

P304

592-601

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P31

scholarly article

case report

P356

10.1002/MGG3.305

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Prashant K Verma

Zahurul A Bhuiyan

P577

2017-06-21T00:00:00Z

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P698

28944242

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P932

5606890

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