Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Periventricular Heterotopia[original query] |
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Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders. PloS one 2017 9 12 (9): e0185103. González-Morón Dolores, Vishnopolska Sebastián, Consalvo Damián, Medina Nancy, Marti Marcelo, Córdoba Marta, Vazquez-Dusefante Cecilia, Claverie Santiago, Rodríguez-Quiroga Sergio Alejandro, Vega Patricia, Silva Walter, Kochen Silvia, Kauffman Marcelo Andr |
Epilepsy phenotypes associated with MAP1B-related brain malformations. Epileptic disorders : international epilepsy journal with videotape 2021 3 23 (2): 392-396. Arya Ravindra, Spaeth Christine, Zhang Wenyi |
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- Page last updated:Apr 22, 2024
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