作者: Fu-Hai Lin , Ruth Lin , Henryk M. Wisniewski , Yu-Wen Hwang , Inge Grundke-Iqbal
DOI: 10.1016/S0006-291X(05)80136-6
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摘要: Summary Point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 (ND2) were detected 10 19 Alzheimer's brains but not 11 normal brains. The same also 6 patients with amyotrophic lateral sclerosis (ALS). However, neurofibrillary tangles and neuritic plaques characteristic disease found histologically the brain one ALS patient who was positive mutation. finding suggests that a point mutation ND2 is potential risk factor for disease.