Litt M - Search Results

1

A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation.

Hershberger RE, Hanson EL, Jakobs PM, Keegan H, Coates K, Bousman S, Litt M. Hershberger RE, et al. Among authors: litt m. Am Heart J. 2002 Dec;144(6):1081-6. doi: 10.1067/mhj.2002.126737. Am Heart J. 2002. PMID: 12486434

2

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.

Hershberger RE, Parks SB, Kushner JD, Li D, Ludwigsen S, Jakobs P, Nauman D, Burgess D, Partain J, Litt M. Hershberger RE, et al. Among authors: litt m. Clin Transl Sci. 2008 May;1(1):21-6. doi: 10.1111/j.1752-8062.2008.00017.x. Clin Transl Sci. 2008. PMID: 19412328 Free PMC article.

3

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Peterson A, Li D, Jakobs P, Litt M, Porter CB, Rahko PS, Hershberger RE. Parks SB, et al. Among authors: litt m. Am Heart J. 2008 Jul;156(1):161-9. doi: 10.1016/j.ahj.2008.01.026. Epub 2008 Mar 12. Am Heart J. 2008. PMID: 18585512 Free PMC article.

4

Mutations of presenilin genes in dilated cardiomyopathy and heart failure.

Li D, Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Partain J, Nixon RR, Allen CN, Irwin RP, Jakobs PM, Litt M, Hershberger RE. Li D, et al. Among authors: litt m. Am J Hum Genet. 2006 Dec;79(6):1030-9. doi: 10.1086/509900. Epub 2006 Oct 24. Am J Hum Genet. 2006. PMID: 17186461 Free PMC article.

5

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.

Hanson EL, Jakobs PM, Keegan H, Coates K, Bousman S, Dienel NH, Litt M, Hershberger RE. Hanson EL, et al. Among authors: litt m. J Card Fail. 2002 Feb;8(1):28-32. doi: 10.1054/jcaf.2002.31157. J Card Fail. 2002. PMID: 11862580

6

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

7

A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.

Kramer P, Yount J, Mitchell T, LaMorticella D, Carrero-Valenzuela R, Lovrien E, Maumenee I, Litt M. Kramer P, et al. Among authors: litt m. Genomics. 1996 Aug 1;35(3):539-42. doi: 10.1006/geno.1996.0395. Genomics. 1996. PMID: 8812489 Free article.

8

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.

9

Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2.

Litt M, Carrero-Valenzuela R, LaMorticella DM, Schultz DW, Mitchell TN, Kramer P, Maumenee IH. Litt M, et al. Hum Mol Genet. 1997 May;6(5):665-8. doi: 10.1093/hmg/6.5.665. Hum Mol Genet. 1997. PMID: 9158139

10

Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women.

Payami H, Zareparsi S, Montee KR, Sexton GJ, Kaye JA, Bird TD, Yu CE, Wijsman EM, Heston LL, Litt M, Schellenberg GD. Payami H, et al. Among authors: litt m. Am J Hum Genet. 1996 Apr;58(4):803-11. Am J Hum Genet. 1996. PMID: 8644745 Free PMC article.

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