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书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0382958<br><br> <br><br>书目名称Genotype - Proteotype - Phenotype Relationships in Neurodegenerative Diseases读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0382958<br><br> <br><br>挖掘 发表于 2025-3-21 22:13:52
https://doi.org/10.1007/978-3-662-26337-2n APP and PS1 have been described. Second, in rare families with PS1 mutations, there are mutation-bearing individuals who may have escaped clinical disease. Third, some APP mutations alter the sequence of Aβ and lead to severe angiopathy with hemorrhage, rather than the plaques and tangles of AD. F该得 发表于 2025-3-22 02:18:04
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,Early Onset Familial Alzheimer’s Disease: Is a Mutation Predictive of Pathology?,n APP and PS1 have been described. Second, in rare families with PS1 mutations, there are mutation-bearing individuals who may have escaped clinical disease. Third, some APP mutations alter the sequence of Aβ and lead to severe angiopathy with hemorrhage, rather than the plaques and tangles of AD. FUrgency 发表于 2025-3-23 07:41:16
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