Publication | Closed Access
Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms
50
Citations
37
References
2004
Year
Genetic DisorderRett SyndromeGeneticsHuman PolymorphismPathologyMolecular GeneticsDisease Gene IdentificationMedicineEpigeneticsPathological MutationsJapanese PatientsClinical Genetics
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