AB129. Prevalence of ATP7B mutation hotspots in Thai population

BACKGROUND: Wilson disease (WD), an autosomal recessive disorder, is a disease which effects copper excretion from liver, leading to copper deposit in many organs like liver, central nervous system and skin. This disease is one of a common genetic disorder which carrier prevalence approximate one in...

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Vydáno v:Ann Transl Med
Hlavní autoři: Kunakorn, Boonyawish, Chitphuk, Sermsiri, Boosabaratana, Manisa, Tunteeratum, Atchara, Sura, Thanyachai, Dejsuphong, Donniphat
Médium: Artigo
Jazyk:Inglês
Vydáno: AME Publishing Company 2017
Témata:
Molecular Genetics, Genomics, Mechanisms of Diseases
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641783/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s129
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