Publications

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Author Title [ Year(Desc)]
Filters: Author is Pehlivan, Davut and Keyword is High-Throughput Nucleotide Sequencing  [Clear All Filters]
2015
Pehlivan, D. et al. Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis. Hum Genet 134, 671-3 (2015).
2016
Pehlivan, D. et al. The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy. Genet Med 18, 443-51 (2016).