Southern transfer protocol for confirmation of Huntington disease

Clinical Chemistry

Volumn 42, Issue 10, 1996, Pages 1711-1712

  Guida, Marco ^a   Fenwick, Raymond G ^b   Papp, Audrey C ^a   Snyder, Pamela J ^a   Sedra, Mary ^a   Prior, Thomas W ^a  

^a OHIO STATE UNIVERSITY   (United States)

^b QUEST DIAGNOSTICS NICHOLS INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SEQUENCE; ARTICLE; AUTORADIOGRAPHY; CLINICAL PROTOCOL; GENE AMPLIFICATION; HUNTINGTON CHOREA; POLYMERASE CHAIN REACTION; TANDEM REPEAT;

EID: 0029903690     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/42.10.1711     Document Type: Article

References (7)

1. Martin JB, Gusella JF. Huntington's disease: pathogenesis and management. N Engl J Med 1986;315:1267-76.
2. The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993;72:971-83.
3. Andrew SE, Goldberg YP, Kremer B, Telenius H, Theilmann J, Adam S, et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nature Genet 1993;4:398-403.
4. Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, Frontali M, et al. Trinucleotide repeat length instability and age of onset in Huntington's disease. Nature Genet 1993;4:387-92.
5. Snell RG, MacMillan JC, Cheadle JP, Fenton I, Lazarou LP, Davies P, et al. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nature Genet 1993;4:393-7.
6. Andrew SE, Goldberg YP, Theilmann J, Zeisler J, Hayden MR. A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing. Hum Mol Genet 1994;3:65-67.
7. Guida M, Marger RS, Papp AC, Snyder PJ, Sedra MS, Kissel JT. et al. A molecular protocol for diagnosing myotonic dystrophy. Clin Chem 1995;41:69-72.