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[Therefore, we propose that ABCC9 mutations lead to a spectrum of phenotypes formerly known as CantĂș syndrome, HAFF and AFA, which may not be clearly distinguishable by clinical criteria, and that all patients with clinical signs belonging to this spectrum should be revisited and offered ABCC9 mutation analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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