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Homozygous missense STRADA mutation in a patient with polyhydramnios, megalencephaly and symptomatic epilepsy syndrome

Aerden, Mioa; Vallaeys, Loreb; Holvoet, Maureena; De Waele, Liesbethc,,d; Van Den Bogaert, Krisa; Devriendt, Koena

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doi: 10.1097/MCD.0000000000000368
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