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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Query Trace: Syndrome and CLDN14[original query]
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.
Clinical genetics 2016 Sep .
Faridi Rabia, Rehman Atteeq U, Morell Robert J, Friedman Penelope L, Demain Leigh, Zahra Sana, Khan Asma Ali, Tohlob Dalia, Assir Muhammad Zaman, Beaman Glenda, Khan Shaheen N, Newman William G, Riazuddin Sheikh, Friedman Thomas
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