Human Genome Epidemiology Literature Finder
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Query Trace: ATP9A[original query] |
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Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families. Current issues in molecular biology 2021 12 43 (3): 1778-1793. Fazia Teresa, Marzanati Daria, Carotenuto Anna Laura, Beecham Ashley, Hadjixenofontos Athena, McCauley Jacob L, Saddi Valeria, Piras Marialuisa, Bernardinelli Luisa, Gentilini Davi |
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- Page last updated:Mar 18, 2024
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