Evidence of somatic mosaicism for a MECP2 mutation in females with Rett syndrome: diagnostic implications

समान संसाधन

• De novo mosaic MECP2 mutation in a female with Rett syndrome
  द्वारा: Alexandrou, Angelos, और अन्य
  प्रकाशित: (2019)
• Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease
  द्वारा: Villard, L., और अन्य
  प्रकाशित: (2001)
• Mutations in the MECP2 gene in a cohort of girls with Rett syndrome
  द्वारा: HAMPSON, K., और अन्य
  प्रकाशित: (2000)
• Persistent Unresolved Inflammation in the Mecp2-308 Female Mutated Mouse Model of Rett Syndrome
  द्वारा: Alessio Cortelazzo, और अन्य
  प्रकाशित: (2017-01-01)
• Persistent Unresolved Inflammation in the Mecp2-308 Female Mutated Mouse Model of Rett Syndrome
  द्वारा: Cortelazzo, Alessio, और अन्य
  प्रकाशित: (2017)