An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family

समान संसाधन

• Characterization of Novel MSX1 Mutations Identified in Japanese Patients with Nonsyndromic Tooth Agenesis
  द्वारा: Yamaguchi, Seishi, और अन्य
  प्रकाशित: (2014)
• WNT10A variants isolated from Japanese patients with congenital tooth agenesis
  द्वारा: Machida, Junichiro, और अन्य
  प्रकाशित: (2017)
• Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia
  द्वारा: Kamamoto, Munefumi, और अन्य
  प्रकाशित: (2011)
• A novel PITX2 mutation causing iris hypoplasia
  द्वारा: Kimura, Masashi, और अन्य
  प्रकाशित: (2014)
• Novel MSX1 frameshift mutation in a Japanese family with nonsyndromic oligodontia
  द्वारा: Adachi, Junya, और अन्य
  प्रकाशित: (2021)