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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Novel human pathological mutations. Gene symbol: ABCD1. Disease: X-linked adrenoleukodystrophy
Cyntia Anabel Amorosi1, Helena Treslova, Raquel Dodelson de Kremer
1Center for Study of Inborn Errors of Metabolism, CEMECO, Pediatric Clinical Department, Children's Hospital and National University of Cordoba, Córdoba, Argentinia. cytiam@hotmail.com
Human Genetics
|April 14, 2011
Abstract
No abstract available in PubMed .
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