Concepedia

Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter:

Melanie A. Knight, Marina Kennerson, Richard Anney, Tohru Matsuura, Garth A. Nicholson, Peyman Salimi-Tari, R. J McKinlay Gardner, Elsdon Storey, Susan M. Forrest

Neurobiology of Disease · 2003 · 69 citations · 53 references

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References

53

Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

, , +16

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel

Olga Zhuchenko, Jennifer M. Bailey, Penelope E. Bonnen et al. · Nature Genetics · 1997 · 1.6K citations

, , +16

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

David P. Kelsell, John Dunlop, Howard P. Stevens et al. · Nature · 1997 · 1.5K citations

, , +13

A routine method for the establishment of permanent growing lymphoblastoid cell lines

Heidemarie Neitzel · Human Genetics · 1986 · 647 citations

, , +13

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

Michael D. Koob, Melinda L. Moseley, Lawrence J. Schut et al. · Nature Genetics · 1999 · 639 citations

, , +13