TY  - CHAP
M1  - Book, Section
TI  - Wilson’s Disease
A1  - Brewer, George J.
A2  - Jameson, J. Larry
A2  - Fauci, Anthony S.
A2  - Kasper, Dennis L.
A2  - Hauser, Stephen L.
A2  - Longo, Dan L.
A2  - Loscalzo, Joseph
PY  - 2018
T2  - Harrison's Principles of Internal Medicine, 20e
AB  - Wilson’s  disease  is  an  autosomal  recessive  disorder  caused  by  mutations  in  the  ATP7B  gene,  which  encodes  a  membrane-bound,  copper-transporting  ATPase.  Clinical  manifestations  are  caused  by  copper  toxicity  and  primarily  involve  the  liver  and  the  brain.  Because  effective  treatment  is  available,  it  is  important  to  make  this  diagnosis  early.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/23
UR  - accessmedicine.mhmedical.com/content.aspx?aid=1156564106
ER  -