https://www.selleckchem.com/pr....oducts/SB-431542.htm
d inflammation. To test the hypothesis that many patients presenting with congenital insensitivity to pain have lesser known or unidentified mutations not captured by conventional genetic panels, we performed whole-exome sequencing in a cohort of well-characterized patients with a clinical diagnosis of congenital hereditary sensory and autonomic neuropathy with unrevealing conventional genetic testing. We performed whole-exome sequencing (WES) in 13 patients with congenital impaired or absent sensation to pain and temperature with no
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