Copy number variation (CNV) identification and association study on 3,928 Alzheimer’s disease whole genome sequencing data from the Alzheimer’s Disease Sequencing Project (ADSP)

Copy number variation (CNV) identification and association study on 3,928 Alzheimer’s disease whole genome sequencing data from the Alzheimer’s Disease Sequencing Project (ADSP)

Background Estimation of heritability of Alzheimer’s Disease (AD) ranges from 49‐79%, but the conventional single nucleotide variants (SNVs) identified to date account for

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Veröffentlicht in:Alzheimer's & dementia 2021-12, Vol.17, p.e052721-n/a
Hauptverfasser: Lee, Wan‐Ping, Conery, Mitchell, Valladares, Otto, Chou, Yi‐Fan, Leung, Yuk Yee, Kuzma, Amanda B, Tucci, Albert A, Brucker, Amanda, Lu, Wenbin, Schellenberg, Gerard D., Wang, Li‐San, Tzeng, Jung‐Ying
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Sprache:eng
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Zusammenfassung:Background Estimation of heritability of Alzheimer’s Disease (AD) ranges from 49‐79%, but the conventional single nucleotide variants (SNVs) identified to date account for
ISSN:1552-5260
1552-5279
DOI:10.1002/alz.052721