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: | Article |
| Language: | English |
| Published: |
Pediatric Neurology Briefs Publishers
2005-08-01
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| Series: | Pediatric Neurology Briefs |
| Subjects: | |
| Online Access: | https://www.pediatricneurologybriefs.com/articles/1252 |
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