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August 10, 2015International Journal of Developmental NeuroscienceOpen Access

Variant Rett syndrome in a girl with a pericentric X‐chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene

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Authors

JVJosé Pedro VieiraHospital de Dona EstefâniaFLFátima LopesIrRADIAREASAnabela Silva‐FernandesUniversity of Luxembourg

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Vieira et al. (2015) studied this question.

synapsesocial.com/papers/6aa226e053426e2d6db2b244https://doi.org/10.1016/j.ijdevneu.2015.07.010
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