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Filters: Author is Çağlayan, Ahmet O and Keyword is High-Throughput Nucleotide Sequencing  [Clear All Filters]
2016
Çağlayan, A. O. et al. A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP. J Hum Genet 61, 395-403 (2016).