Publication | Open Access
Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes
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Citations
22
References
2010
Year
Mendelian DisorderGenetic DisorderRett SyndromeGeneticsMecp2 MutationsPathologyMolecular GeneticsDisease Gene IdentificationMedicineVariant InterpretationClinical Genetics
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