Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

類似資料

• MECP2 Mutations in People without Rett Syndrome
  著者:: Suter, Bernhard, 等
  出版事項: (2014)
• Diagnostic Testing for Rett Syndrome by DHPLC and Direct Sequencing Analysis of the MECP2 Gene: Identification of Several Novel Mutations and Polymorphisms
  著者:: Buyse, Inge M., 等
  出版事項: (2000)
• Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice
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  出版事項: (2014)
• Enrichment of mutations in chromatin regulators in people with Rett Syndrome lacking mutations in MECP2
  著者:: Sajan, Samin A., 等
  出版事項: (2016)
• Detection of Rarely Identified Multiple Mutations in MECP2 Gene Do Not Contribute to Enhanced Severity in Rett Syndrome
  著者:: Chapleau, Christopher A., 等
  出版事項: (2013)