一个具有 K17I ANG 突变的大型 FALS 家系中 ALS - FTD 病例。
Mesh : Aged Amino Acid Sequence Amino Acid Substitution Amyotrophic Lateral Sclerosis / complications genetics Base Sequence Dementia / complications genetics Female Heterozygote Humans Isoleucine Lysine Male Middle Aged Mutation Pedigree Ribonuclease, Pancreatic / genetics
来 源: DOI:10.1212/01.wnl.0000339487.84908.00