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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Format: | Book |
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Pediatric Neurology Briefs Publishers,
2005-08-01T00:00:00Z.
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A1234.567 |
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