Homozygous c.1160C>T (P38L) in the MECP2 gene in a female Rett syndrome patient. [electronic resource]

By: Contributor(s): Producer: 20160913Description: 127-9 p. digitalISSN:
  • 1532-2653
Subject(s): Online resources: In: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia vol. 25
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Publication Type: Case Reports; Journal Article

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