Title : ACE gene missense mutation in a case with early-onset, rapid progressing dementia.

Pub. Date : 2019

PMID : 31673674






2 Functional Relationships(s)
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1 Genetic testing has revealed the presence of genetic mutations (c.A479G, p.N160S) of ACE, which causes the 160th codon of the ACE protein to change from aspartic acid to serine, and at the same time genotype of apolipoprotein E (APOE) is e3/e4. cholecystokinin C-terminal flanking peptide angiotensin I converting enzyme Homo sapiens
2 Genetic testing has revealed the presence of genetic mutations (c.A479G, p.N160S) of ACE, which causes the 160th codon of the ACE protein to change from aspartic acid to serine, and at the same time genotype of apolipoprotein E (APOE) is e3/e4. cholecystokinin C-terminal flanking peptide angiotensin I converting enzyme Homo sapiens