6 research outputs found
Development of devices for beam divergence correction in the high-resolution NRSE spectrometer
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Biological Monitoring of Styrene in FRPāMaking Small Industries in Kumamoto, JapanāWinterāSummer Difference and Effect of Protective Masks in Practical Working Conditionsā
No full textShield evaluation of cold neutron curved guide tubes for J-PARC neutron resonance spin echo spectrometers
No full textThe APOA1 p.Leu202Arg variant potentially causes autosomal recessive cardiac amyloidosis
Get PDFApoA-I amyloidosis is an extremely rare form of systemic amyloidosis that commonly involves the heart, kidneys, and liver. ApoA-I amyloidosis is caused by amyloidogenic variants of APOA1 that are inherited in an autosomal dominant manner. Here, we report a 69-year-old man with sporadic cardiac amyloidosis who was born to consanguineous parents and carried a homozygous variant of p.Leu202Arg in APOA1
