Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family

مواد مشابهة

• A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family
  بواسطة: Naseer, Muhammad Imran, وآخرون
  منشور في: (2017)
• Exome sequencing reveled a compound heterozygous mutations in RTTN gene causing developmental delay and primary microcephaly
  بواسطة: Imran Naseer, Muhammad, وآخرون
  منشور في: (2021)
• Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family
  بواسطة: Naseer, Muhammad I., وآخرون
  منشور في: (2018)
• Next generation sequencing reveals novel homozygous frameshift in PUS7 and splice acceptor variants in AASS gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephaly
  بواسطة: Naseer, Muhammad Imran, وآخرون
  منشور في: (2020)
• Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly
  بواسطة: Naseer, Muhammad Imran, وآخرون
  منشور في: (2021)