Title : Rapidly Progressive Frontotemporal Dementia Associated with MAPT MutationĀ G389R.

Pub. Date : 2017

PMID : 27802239






2 Functional Relationships(s)
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1 Genetic testing revealed a heterozygous guanine to cytosine mutation at the first base of codon 389 (c.1165G>A) of MAPT, the tau gene, resulting in a glycine to arginine substitution in the patient and two unaffected relatives. Arginine microtubule associated protein tau Homo sapiens
2 Genetic testing revealed a heterozygous guanine to cytosine mutation at the first base of codon 389 (c.1165G>A) of MAPT, the tau gene, resulting in a glycine to arginine substitution in the patient and two unaffected relatives. Arginine microtubule associated protein tau Homo sapiens