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Article

WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal period

26 Feb 2015

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25716914
DOI: 10.1038/jhg.2015.17

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WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal periodPMID 25716914Read ↗

Epilepsy and mental retardation restricted to females: X-linked epileptic infantile encephalopathy of unusual inheritanceSemantic proximity Read ↗

Early onset epileptic encephalopathy caused by novel compound heterozygous mutation of WWOX gene.Semantic proximity Read ↗

WWOXdevelopmental and epileptic encephalopathy: Understanding the epileptology and the mortality riskSemantic proximity Read ↗

<em>WWOX </em>Gene Disease as Infantile Catastrophic Epileptic Encephalopathy (WOREE Syndrome Plus): A Comprehensive Case Study with Brief Literature UpdateSemantic proximity Read ↗

Practical clues for diagnosing WWOX encephalopathy.Semantic proximity Read ↗

Developmental epileptic encephalopathy caused by homozygosity of a c.172+1G>C variant in the WWOX gene.Semantic proximity Read ↗

[Genotype and phenotype of WWOX gene related developmental and epileptic encephalopathy].Semantic proximity Read ↗

Novel homozygous mutation in the WWOX gene causes seizures and global developmental delay: Report and reviewSemantic proximity Read ↗

Severe CNS involvement in WWOX mutations: Description of five new cases.Semantic proximity Read ↗

Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutations.Semantic proximity Read ↗

W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report.Semantic proximity Read ↗

Novel compound heterozygous mutations in the WWOX gene cause early infantile epileptic encephalopathy.Semantic proximity Read ↗

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