Author Archives: Iqra Mumal, MSc

Japanese Find Another Mutation That Could Lead to Fabry Disease

A newborn screening study led to Japanese researchers discovering another mutation that may cause Fabry disease. The study, “A new mutation found in newborn screening for Fabry disease evaluated by plasma globotriaosylsphingosine levels,” was published in the Official Journal of the Japan Society of Human Genetics. Fabry disease…