Genetic Analysis of Hereditary Transthyretin Ala97Ser Related AmyloidosisHui-Ching Hsu 1, Ming-Feng Liao 2, Jung-Lung Hsu 2, Yun-Lin Lee 2, Long-Sun Ro 2
1Department of Traditional Chinese Medicine, Division of Chinese Acupuncture and Traumatology, Chang Gung Memorial Hospital Linkou Medical Center and Chang Gung University College of Medicine, 2Department of Neurology, Chang Gung Memorial Hospital Linkou Medical Center and Chang Gung University College of Medicine
Here, we present a protocol to confirm the presence of point mutation for the diagnosis of hereditary transthyretin amyloidosis, using Ala97Ser, the most common endemic mutation in Taiwan, as an example.