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Targeted exon sequencing fails to identify rare coding variants with large effect in rheumatoid arthritis
INTRODUCTION: Although it has been suggested that rare coding variants could explain the substantial missing heritability, very few sequencing studies have been performed in rheumatoid arthritis (RA). We aimed to identify novel functional variants with rare to low frequency using targeted exon seque...
Autores principales: | Bang, So-Young, Na, Young-Ji, Kim, Kwangwoo, Joo, Young Bin, Park, Youngho, Lee, Jaemoon, Lee, Sun-Young, Ansari, Adnan A, Jung, Junghee, Rhee, Hwanseok, Lee, Jong-Young, Han, Bok-Ghee, Ahn, Sung-Min, Won, Sungho, Lee, Hye-Soon, Bae, Sang-Cheol |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203956/ https://www.ncbi.nlm.nih.gov/pubmed/25267259 http://dx.doi.org/10.1186/s13075-014-0447-7 |
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