T. Conrad Gilliam to Hepatolenticular Degeneration
This is a "connection" page, showing publications T. Conrad Gilliam has written about Hepatolenticular Degeneration.
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0.548
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Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation. Hum Mol Genet. 1999 Sep; 8(9):1665-71.
Score: 0.168
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Arm tremor secondary to Wilson's disease. Mov Disord. 1998 Mar; 13(2):351-3.
Score: 0.151
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Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions. Hum Mol Genet. 1994 Sep; 3(9):1647-56.
Score: 0.119
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Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses. Am J Hum Genet. 1997 Aug; 61(2):317-28.
Score: 0.036
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An international symposium on Wilson's and Menkes' diseases. Hepatology. 1996 Oct; 24(4):952-8.
Score: 0.034
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Genetic disorders of copper metabolism. Curr Opin Pediatr. 1994 Dec; 6(6):698-701.
Score: 0.030
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Heterologous expression of the metal-binding domains of human copper-transporting ATPases (P1-ATPases). Ann N Y Acad Sci. 1997 Nov 03; 834:155-7.
Score: 0.009