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Diagnosis of Human Axillary Osmidrosis by Genotyping of the Human ABCC11 Gene: Clinical Practice and Basic Scientific Evidence
The importance of personalized medicine and healthcare is becoming increasingly recognized. Genetic polymorphisms associated with potential risks of various human genetic diseases as well as drug-induced adverse reactions have recently been well studied, and their underlying molecular mechanisms are...
Autores principales: | Toyoda, Yu, Gomi, Tsuneaki, Nakagawa, Hiroshi, Nagakura, Makoto, Ishikawa, Toshihisa |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4781944/ https://www.ncbi.nlm.nih.gov/pubmed/27057547 http://dx.doi.org/10.1155/2016/7670483 |
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