Genetic analysis of ATP7B in 102 south Indian families with Wilson disease

Wilson disease (WD) is an autosomal recessive disorder, characterized by excessive deposition of copper in various parts of the body, mainly in the liver and brain. It is caused by mutations in ATP7B. We report here the genetic analysis of 102 WD families from a south Indian population. Thirty-six d...

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Detalles Bibliográficos
Autores principales: Singh, Nivedita, Kallollimath, Pradeep, Shah, Mohd Hussain, Kapoor, Saketh, Bhat, Vishwanath Kumble, Viswanathan, Lakshminarayanapuram Gopal, Nagappa, Madhu, Bindu, Parayil S., Taly, Arun B., Sinha, Sanjib, Kumar, Arun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502322/
https://www.ncbi.nlm.nih.gov/pubmed/31059521
http://dx.doi.org/10.1371/journal.pone.0215779

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502322/
https://www.ncbi.nlm.nih.gov/pubmed/31059521
http://dx.doi.org/10.1371/journal.pone.0215779

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