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A Haptoglobin Exon Copy Number Variant Associates With HIV-Associated Neurocognitive Impairment in European and African-Descent Populations

A common two-exon deletion distinguishes the gene encoding the free hemoglobin capturing protein—haptoglobin (HP)–into two alleles: HP1 and HP2. To evaluate the impact of this copy number variant (CNV) on neurocognitive impairment (NCI) in people living with HIV, we imputed this variant in 432 Europ...

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Detalles Bibliográficos
Autores principales:	Bai, Haimeng, Kaur, Harpreet, Kallianpur, Asha R., Hulgan, Todd, Franklin, Donald R., Letendre, Scott L., Ellis, Ronald J., Bush, William S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727522/ https://www.ncbi.nlm.nih.gov/pubmed/35003209 http://dx.doi.org/10.3389/fgene.2021.756685

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