Cortical atrophy in presymptomatic Alzheimer's disease presenilin 1 mutation carriers. [electronic resource]
Producer: 20130531Description: 556-61 p. digitalISSN:- 1468-330X
- Adult
- Alzheimer Disease -- genetics
- Atrophy
- Cerebral Cortex -- pathology
- DNA -- genetics
- Female
- Heterozygote
- Humans
- Magnetic Resonance Imaging
- Male
- Memory -- physiology
- Mental Recall -- physiology
- Mutation -- genetics
- Neuropsychological Tests
- Presenilin-1 -- genetics
- Recognition, Psychology -- physiology
- Socioeconomic Factors
- Verbal Behavior -- physiology
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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