A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome
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| Description | scientific article |
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author: Hatem El-shanti Pedro Gonzalez-Alegre Robyn Wallace Marcus Nashelsky Diane C Slusarski Jeffrey Axelrod Amos D. Korczyn Samuel Berkovic |
| Publication date | October 30, 2008 |
| Language | English |
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