Pediatric Neurology Briefs (Aug 2005)

ABCD1 Gene Mutations in Chinese Patients with ALD

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-19-8-5
Journal volume & issue
Vol. 19, no. 8
pp. 60 – 60

Abstract

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Thirty-two different ABCD1 mutations were identified by direct sequencing of polymerase chain reaction products in 34 unrelated Chinese X-linked adrenoleukodystrophy (ALD) patients examined at Peking University First Hospital, Beijing, PRC.

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