ABCD1 Gene Mutations in Chinese Patients with ALD

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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Bibliographic Details
Main Author: J Gordon Millichap (Author)
Format: Book
Published: Pediatric Neurology Briefs Publishers, 2005-08-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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