R778L, H1069Q, and I1102T mutation study in neurologic Wilson disease.

Kalita, Jayantee

R778L, H1069Q, and I1102T mutation study in neurologic Wilson disease. [electronic resource] - Neurology India - 627-30 p. digital

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

0028-3886

10.4103/0028-3886.68678 doi


Adenosine Triphosphatases--genetics
Adolescent
Adult
Amino Acids--genetics
Cation Transport Proteins--genetics
Child
Child, Preschool
Copper-Transporting ATPases
DNA Mutational Analysis--methods
Family Health
Female
Gene Frequency
Hepatolenticular Degeneration--genetics
Humans
India
Magnetic Resonance Imaging--methods
Male
Mutation--genetics
Severity of Illness Index
Young Adult