Rare coding variants pinpoint genes that control human hematological traits

The identification of rare coding or splice site variants remains the most straightforward strategy to link genes with human phenotypes. Here, we analyzed the association between 137,086 rare (minor allele frequency (MAF) <1%) coding or splice site variants and 15 hematological traits in up to 30...

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Dettagli Bibliografici
Pubblicato in:PLoS Genet
Autori principali: Mousas, Abdou, Ntritsos, Georgios, Chen, Ming-Huei, Song, Ci, Huffman, Jennifer E., Tzoulaki, Ioanna, Elliott, Paul, Psaty, Bruce M., Auer, Paul L., Johnson, Andrew D., Evangelou, Evangelos, Lettre, Guillaume, Reiner, Alexander P.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2017
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5560754/
https://ncbi.nlm.nih.gov/pubmed/28787443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1006925
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