Confirmatory Results
Identifying highly-penetrant disease causal mutations using next generation sequencing: Guide to whole process
View ORCID ProfileMesut Erzurumluoglu
doi: https://doi.org/10.1101/011130
Mesut Erzurumluoglu
1Bristol Genetic Epidemiology Laboratories (BGEL), School of Social and Community Medicine, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, United Kingdom.
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Posted November 06, 2014.
Identifying highly-penetrant disease causal mutations using next generation sequencing: Guide to whole process
Mesut Erzurumluoglu
bioRxiv 011130; doi: https://doi.org/10.1101/011130
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