A novel ATP7B gene mutation in a liver failure patient with normal ceruloplasmin and low serum alkaline phosphatase

Gene

Volumn 538, Issue 1, 2014, Pages 204-206

  Chen, Li ^a   Li, Xinhua ^b   Zheng, Zhiyong ^c   Lu, Xujiang ^a   Lin, Minghua ^a   Pan, Chen ^a   Liu, Jingfeng ^a  

^a FUJIAN MEDICAL UNIVERSITY   (China)

^b THE THIRD AFFILIATED HOSPITAL OF SUN YAT SEN UNIVERSITY   (China)

^c CHINESE PLA GENERAL HOSPITAL   (China)

Author keywords

Genetics; Liver failure; Pathology; Wilson's disease

Indexed keywords

GENETICS; LIVER FAILURE; PATHOLOGY; WILSON'S DISEASE;

ADENOSINE TRIPHOSPHATASES; ADULT; ALKALINE PHOSPHATASE; CATION TRANSPORT PROTEINS; CERULOPLASMIN; FEMALE; HEPATOLENTICULAR DEGENERATION; HUMANS; LIVER FAILURE; MUTATION;

EID: 84893717445     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2013.10.044     Document Type: Article

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