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Victoria Harrison, Lyndsey Connell, Jesse Hayesmoore, Joanna McParland, Michael G. Pike and Edward Blair Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters American Journal of Medical Genetics Part A 155

Article first published online: 30 SEP 2011 | DOI: 10.1002/ajmg.a.34255

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