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...

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Detalles Bibliográficos
Autores principales: Toyoda, Yu, Gomi, Tsuneaki, Nakagawa, Hiroshi, Nagakura, Makoto, Ishikawa, Toshihisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Review Article
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

Internet

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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