ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients.

Santhosh, S

ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients. [electronic resource] - Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology - 277-82 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0254-8860


Adenosine Triphosphatases--genetics
Adolescent
Adult
Age of Onset
Cation Transport Proteins--genetics
Ceruloplasmin--analysis
Child
Codon
Consanguinity
Copper--urine
Copper-Transporting ATPases
Exons
Female
Hepatolenticular Degeneration--genetics
Humans
India
Male
Middle Aged
Mutation
Phenotype
Polymorphism, Genetic