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Two recent case reports on BHD – Epidemiologic study of patients in Asia and new FLCN mutation

Furuya et al. (2016) present a new study describing genetic, epidemiologic and clinicopathologic features of 312 Asian individuals with BHD manifestations based on data from 120 probands from different families (119 Japanese and 1 Taiwanese), 36 siblingss with genetic testing and 156 siblings without genetic testing. Among the 120 probands that were grouped as ‘Possible […]


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