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Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome
Carla Caffarelli, Stefano Gonnelli, Maria Dea Tomai Pitinca and 4 more
BMC Medical Genetics · 2020
Cited by papers we hold 1
- MeCP2: The Genetic Driver of Rett Syndrome Epigenetics · 2021No notice
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