Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ashcroft F. M., Röper J. Transporters, channels and human disease. Curr Opin Cell Biol. 1993 Aug;5(4):677–683. doi: 10.1016/0955-0674(93)90139-h. [DOI] [PubMed] [Google Scholar]
- Bain P. G., O'Brien M. D., Keevil S. F., Porter D. A. Familial periodic cerebellar ataxia: a problem of cerebellar intracellular pH homeostasis. Ann Neurol. 1992 Feb;31(2):147–154. doi: 10.1002/ana.410310205. [DOI] [PubMed] [Google Scholar]
- Baloh R. W., Winder A. Acetazolamide-responsive vestibulocerebellar syndrome: clinical and oculographic features. Neurology. 1991 Mar;41(3):429–433. doi: 10.1212/wnl.41.3.429. [DOI] [PubMed] [Google Scholar]
- Bell G. I., Karam J. H., Rutter W. J. Polymorphic DNA region adjacent to the 5' end of the human insulin gene. Proc Natl Acad Sci U S A. 1981 Sep;78(9):5759–5763. doi: 10.1073/pnas.78.9.5759. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Buetow K. H., Weber J. L., Ludwigsen S., Scherpbier-Heddema T., Duyk G. M., Sheffield V. C., Wang Z., Murray J. C. Integrated human genome-wide maps constructed using the CEPH reference panel. Nat Genet. 1994 Apr;6(4):391–393. doi: 10.1038/ng0494-391. [DOI] [PubMed] [Google Scholar]
- Gancher S. T., Nutt J. G. Autosomal dominant episodic ataxia: a heterogeneous syndrome. Mov Disord. 1986;1(4):239–253. doi: 10.1002/mds.870010404. [DOI] [PubMed] [Google Scholar]
- Gyapay G., Morissette J., Vignal A., Dib C., Fizames C., Millasseau P., Marc S., Bernardi G., Lathrop M., Weissenbach J. The 1993-94 Généthon human genetic linkage map. Nat Genet. 1994 Jun;7(2 Spec No):246–339. doi: 10.1038/ng0694supp-246. [DOI] [PubMed] [Google Scholar]
- Joutel A., Bousser M. G., Biousse V., Labauge P., Chabriat H., Nibbio A., Maciazek J., Meyer B., Bach M. A., Weissenbach J. A gene for familial hemiplegic migraine maps to chromosome 19. Nat Genet. 1993 Sep;5(1):40–45. doi: 10.1038/ng0993-40. [DOI] [PubMed] [Google Scholar]
- Litt M., Hauge X., Sharma V. Shadow bands seen when typing polymorphic dinucleotide repeats: some causes and cures. Biotechniques. 1993 Aug;15(2):280–284. [PubMed] [Google Scholar]
- Litt M., Kramer P., Browne D., Gancher S., Brunt E. R., Root D., Phromchotikul T., Dubay C. J., Nutt J. A gene for episodic ataxia/myokymia maps to chromosome 12p13. Am J Hum Genet. 1994 Oct;55(4):702–709. [PMC free article] [PubMed] [Google Scholar]
- Ptácek L. Ion channel shake-down. Nat Genet. 1994 Oct;8(2):111–112. doi: 10.1038/ng1094-111. [DOI] [PubMed] [Google Scholar]
- Schäffer A. A., Gupta S. K., Shriram K., Cottingham R. W., Jr Avoiding recomputation in linkage analysis. Hum Hered. 1994 Jul-Aug;44(4):225–237. doi: 10.1159/000154222. [DOI] [PubMed] [Google Scholar]
- Vahedi K., Joutel A., Van Bogaert P., Ducros A., Maciazeck J., Bach J. F., Bousser M. G., Tournier-Lasserve E. A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p. Ann Neurol. 1995 Mar;37(3):289–293. doi: 10.1002/ana.410370304. [DOI] [PubMed] [Google Scholar]
- Zasorin N. L., Baloh R. W., Myers L. B. Acetazolamide-responsive episodic ataxia syndrome. Neurology. 1983 Sep;33(9):1212–1214. doi: 10.1212/wnl.33.9.1212. [DOI] [PubMed] [Google Scholar]
- von Brederlow B., Hahn A. F., Koopman W. J., Ebers G. C., Bulman D. E. Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p. Hum Mol Genet. 1995 Feb;4(2):279–284. doi: 10.1093/hmg/4.2.279. [DOI] [PubMed] [Google Scholar]