A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes
2009 ◽
Vol 85
(1)
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pp. 118-122
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Keyword(s):
2007 ◽
Vol 76
(1)
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pp. 41-48
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1999 ◽
Vol 45
(2)
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pp. 182-188
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Keyword(s):
2018 ◽
Vol 38
(13)
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pp. 3346-3357
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Keyword(s):