A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation

Publisher: John Wiley & Sons Inc

E-ISSN: 1552-4833|176|3|699-702

ISSN: 1552-4825

Source: American Journal Of Medical Genetics Part A, Vol.176, Iss.3, 2018-03, pp. : 699-702

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