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April 13, 2009American Journal of Medical Genetics Part A

Novel exon 1 mutations in MECP2 implicate isoform MeCP2ₑ1 in classical Rett syndrome

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Authors

CSCarol SaundersBMBerge E. MinassianECEva W.C. Chow

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Saunders et al. (2009) studied this question.

synapsesocial.com/papers/6ab4dbcf79b154fae7df74efhttps://doi.org/10.1002/ajmg.a.32776
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