Identification of a Novel Nonsense Mutation in PLA2G6 and Prenatal Diagnosis in a Chinese Family With Infantile Neuroaxonal Dystrophy

New Research: Identification of a Novel Nonsense Mutation in PLA2G6 and Prenatal Diagnosis in a Chinese Family With Infantile Neuroaxonal Dystrophy: Background and Purpose Infantile neuroaxonal dystrophy (INAD) is a subtype of… https://t.co/KnXGksDt99 #Ne