Jervell and Lange-Nielson Syndrome masquerading as intractable epilepsy by Jagdish P Goyal, Alka Sethi, V B Shah

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Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case report by N. Adadi, N. Lahrouchi, R. Bouhouch, I. Fellat, R. Amri, M. Alders, A. Sefiani, C. Bezzina, I. Ratbi

Subjects: “…Jervell and Lange-Nielsen syndrome…”
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GENETIC ASPECTS OF CONGENITAL LONG QT SYNDROME by A. A. Chernova, S. Yu. Nikulina, A. V. Gul'bis

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Novel combinations of variations in KCNQ1 were associated with patients with long QT syndrome or Jervell and Lange-Nielsen syndrome by Nongnong Zhao, Zhengyang Yu, Zhejun Cai, Wenai Chen, Xiaopeng He, Zhaoxia Huo, Xiaoping Lin

Subjects: “…Jervell and Lange-Nielsen Syndrome…”
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Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange‐Nielsen deafness syndrome by Qing Chang, Jianjun Wang, Qi Li, Yeunjung Kim, Binfei Zhou, Yunfeng Wang, Huawei Li, Xi Lin

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Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome by Azam Amirian, Seyed Mohammad Dalili, Zahra Zafari, Siamak Saber, Morteza Karimipour, Vahid Akbari, Amirfarjam Fazelifar, Sirous Zeinali

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Cerebral Seizures in an Adolescent with Jervell and Lange-Nielsen Syndrome: It May Not Be Epilepsy by Joachim Levaux, Nesrine Farhat, Lieve Van Casteren, Saskia Bulk, Marie-Christine Seghaye

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A novel KCNQ1 nonsense variant in the isoform-specific first exon causes both jervell and Lange-Nielsen syndrome 1 and long QT syndrome 1: a case report by Motoi Nishimura, Marehiko Ueda, Ryota Ebata, Emi Utsuno, Takuma Ishii, Kazuyuki Matsushita, Osamu Ohara, Naoki Shimojo, Yoshio Kobayashi, Fumio Nomura

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