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Autor:
Santhosh, Sundaresan, Chundamannil Eapen, Eapen, Ramachandran Velayutham, Shaji, Mammen, Chandy, George, Kurian, George, Chandy
Publikováno v:
Medical science monitor : international medical journal of experimental and clinical research. 13(3)
Wilson's disease (WD) is an autosomal recessive disorder leading to copper overload, mainly in the liver and brain, due to mutations in the ATP7B gene. About 10% of heterozygous carriers of ATP7B gene mutations have decreased serum ceruloplasmin, pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a962cfe5db3fbfa055c6c52251eae781
https://pubmed.ncbi.nlm.nih.gov/17325640
https://pubmed.ncbi.nlm.nih.gov/17325640
