A novel nonsense mutation in leucine-rich, glioma-inactivated-1 gene as the underlying cause of familial temporal lobe epilepsy

Sumaira Kanwal; Da Hye Yoo; Shahzad Tahir; Su Jung Lee; Min Hee Lee; Byung Ok Choi; Ki Wha Chung

doi:10.3988/jcn.2018.14.4.591

A novel nonsense mutation in leucine-rich, glioma-inactivated-1 gene as the underlying cause of familial temporal lobe epilepsy

Sumaira Kanwal
, Da Hye Yoo
, Shahzad Tahir
, Su Jung Lee
, Min Hee Lee
, Byung Ok Choi
, Ki Wha Chung

Department of Neurology

Kongju National University
COMSATS University Islamabad
Subh-e-Nao Hospital

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	591-593
Number of pages	3
Journal	Journal of Clinical Neurology (Korea)
Volume	14
Issue number	4
DOIs	https://doi.org/10.3988/jcn.2018.14.4.591
State	Published - Oct 2018

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10.3988/jcn.2018.14.4.591

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@article{d260fbbd3b0140ccbdf0a7f31e0269c5,

title = "A novel nonsense mutation in leucine-rich, glioma-inactivated-1 gene as the underlying cause of familial temporal lobe epilepsy",

author = "Sumaira Kanwal and Yoo, \{Da Hye\} and Shahzad Tahir and Lee, \{Su Jung\} and Lee, \{Min Hee\} and Choi, \{Byung Ok\} and Chung, \{Ki Wha\}",

year = "2018",

month = oct,

doi = "10.3988/jcn.2018.14.4.591",

language = "English",

volume = "14",

pages = "591--593",

journal = "Journal of Clinical Neurology (Korea)",

issn = "1738-6586",

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T1 - A novel nonsense mutation in leucine-rich, glioma-inactivated-1 gene as the underlying cause of familial temporal lobe epilepsy

AU - Kanwal, Sumaira

AU - Yoo, Da Hye

AU - Tahir, Shahzad

AU - Lee, Su Jung

AU - Lee, Min Hee

AU - Choi, Byung Ok

AU - Chung, Ki Wha

PY - 2018/10

Y1 - 2018/10

UR - https://www.scopus.com/pages/publications/85059189092

U2 - 10.3988/jcn.2018.14.4.591

DO - 10.3988/jcn.2018.14.4.591

M3 - Letter

AN - SCOPUS:85059189092

SN - 1738-6586

VL - 14

SP - 591

EP - 593

JO - Journal of Clinical Neurology (Korea)

JF - Journal of Clinical Neurology (Korea)

IS - 4

ER -

A novel nonsense mutation in leucine-rich, glioma-inactivated-1 gene as the underlying cause of familial temporal lobe epilepsy

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