X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8. [electronic resource]

By: Contributor(s): Producer: 20020918Description: 227-31 p. digitalISSN:
  • 0364-5134
Subject(s): Online resources: In: Annals of neurology vol. 52
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Publication Type: Case Reports; Journal Article

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