Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1D.L. Browne, M. Litt, Stephen T. Gancher et al.|Nature Genetics|1994Cited by 776
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAAM. Litt|Human Molecular Genetics|1998Cited by 447
The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.D. K. Grandy, Olivier Civelli, M. Litt et al.|PubMed|1989Cited by 424
SECONDARY STRUCTURE IN RIBONUCLEIC ACIDSPaul Doty, M. Litt, Helga Boedtker et al.|Proceedings of the National Academy of Sciences|1959Cited by 363
Molecular Genetics of Human Blue Cone MonochromacyJeremy Nathans, Gerald A. Fishman, Carol Davenport et al.|Science|1989Cited by 325