Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family. [electronic resource]

By: Contributor(s): Producer: 20191016Description: 347-350 p. digitalISSN:
  • 1319-6138
Subject(s): Online resources: In: Neurosciences (Riyadh, Saudi Arabia) vol. 23
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Publication Type: Case Reports; Journal Article

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