Pediatric Neurology Briefs
Published 2005 | Version v1.0.0
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ABCD1 Gene Mutations in Chinese Patients with ALD

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Abstract

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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PNB-19-60-a

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Created
2005
When the item was originally created.