Litt M - Search Results

1

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.

Browne DL, Gancher ST, Nutt JG, Brunt ER, Smith EA, Kramer P, Litt M. Browne DL, et al. Among authors: litt m. Nat Genet. 1994 Oct;8(2):136-40. doi: 10.1038/ng1094-136. Nat Genet. 1994. PMID: 7842011

2

A gene for episodic ataxia/myokymia maps to chromosome 12p13.

Litt M, Kramer P, Browne D, Gancher S, Brunt ER, Root D, Phromchotikul T, Dubay CJ, Nutt J. Litt M, et al. Am J Hum Genet. 1994 Oct;55(4):702-9. Am J Hum Genet. 1994. PMID: 7942848 Free PMC article.

3

Dinucleotide repeat polymorphisms near the KCNA6 and KCNA1 loci.

Browne DL, Litt M. Browne DL, et al. Among authors: litt m. Hum Mol Genet. 1994 May;3(5):842. doi: 10.1093/hmg/3.5.842-a. Hum Mol Genet. 1994. PMID: 8081383 No abstract available.

4

Identification of two new KCNA1 mutations in episodic ataxia/myokymia families.

Browne DL, Brunt ER, Griggs RC, Nutt JG, Gancher ST, Smith EA, Litt M. Browne DL, et al. Among authors: litt m. Hum Mol Genet. 1995 Sep;4(9):1671-2. doi: 10.1093/hmg/4.9.1671. Hum Mol Genet. 1995. PMID: 8541859 No abstract available.

5

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.

Litt M, Kramer P, LaMorticella DM, Murphey W, Lovrien EW, Weleber RG. Litt M, et al. Hum Mol Genet. 1998 Mar;7(3):471-4. doi: 10.1093/hmg/7.3.471. Hum Mol Genet. 1998. PMID: 9467006

6

Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci.

Browne D, Barker D, Litt M. Browne D, et al. Among authors: litt m. Hum Mol Genet. 1992 Jun;1(3):213. doi: 10.1093/hmg/1.3.213. Hum Mol Genet. 1992. PMID: 1303184 No abstract available.

7

Microsatellite polymorphisms at the D11S554 and D11S569 loci.

Phromchotikul T, Browne D, Litt M. Phromchotikul T, et al. Among authors: litt m. Hum Mol Genet. 1992 Jun;1(3):214. doi: 10.1093/hmg/1.3.214. Hum Mol Genet. 1992. PMID: 1303185 No abstract available.

8

High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.

Zonana J, Jones M, Browne D, Litt M, Kramer P, Becker HW, Brockdorff N, Rastan S, Davies KP, Clarke A, et al. Zonana J, et al. Among authors: litt m. Am J Hum Genet. 1992 Nov;51(5):1036-46. Am J Hum Genet. 1992. PMID: 1357963 Free PMC article.

9

Dinucleotide repeat polymorphism at the PGK1P1 locus.

Browne DL, Zonana J, Litt M. Browne DL, et al. Among authors: litt m. Nucleic Acids Res. 1992 Mar 11;20(5):1169. doi: 10.1093/nar/20.5.1169-a. Nucleic Acids Res. 1992. PMID: 1549504 Free PMC article.

10

Regional localization of the gene for cardiac muscle actin (ACTC) on chromosome 15q.

Kramer PL, Luty JA, Litt M. Kramer PL, et al. Among authors: litt m. Genomics. 1992 Jul;13(3):904-5. doi: 10.1016/0888-7543(92)90185-u. Genomics. 1992. PMID: 1639426 No abstract available.

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