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[These results indicate that variation in the neurologic phenotype of Sj�gren-Larsson syndrome is not strictly determined by the ALDH3A2 mutation or the biochemical defect as expressed in cultured fibroblasts, but by unidentified epigenetic/environmental factors, gene modifiers, or other mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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