Citations for
1ACTC1, CMH1, CMH11, CMH4, MYBPC3, MYH7, MYL2, MYL3, PRKAG2, TNNI3, TNNT2, TPM1
Shared genetic causes of cardiac hypertrophy in children and adults.
Morita H, Rehm HL, Menesses A, McDonough B, Roberts AE, Kucherlapati R, Towbin JA, Seidman JG, Seidman CE.
N Engl J Med 358(18):1899-908. Epub 2008 Apr 9. 2008
2MYL3
Essential myosin light chain as a target for caspase-3 in failing myocardium.
Moretti A, Weig HJ, Ott T, Seyfarth M, Holthoff HP, Grewe D, Gillitzer A, Bott-Flugel L, Schomig A, Ungerer M, Laugwitz KL.
Proc Natl Acad Sci U S A 99(18):11860-5. 2002
3MYL1, MYL2, MYL3, PITX2
Multiple transcriptional domains, with distinct left and right components, in the atrial chambers of the developing heart.
Franco D, Campione M, Kelly R, Zammit PS, Buckingham M, Lamers WH, Moorman AF.
Circ Res 87(11):984-91. 2000
4CMH8, CMH10, MYL2, MYL3
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle.
Poetter K, et al.
Nat Genet 13 : 63-68. 1996
5MYL3, MYL4
Chromosomal assignment of two myosin alkali light-chain genes encoding the ventricular/slow skeletal muscle isoform and the atrial/fetal muscle isoform (MYL3, MYL4).
Cohen-Haguenauer O, et al.
Hum Genet 81 : 278-282. 1989
6MYL3
Human ventricular/slow twitch myosin alkali light chain gene characterization, sequence, and chromosomal location.
Fodor WL, et al.
J Biol Chem 264 : 2143-2149. 1989
7MYL3
A human myosin alkali light chain gene mapped to chromosome 3.
Darras BT, et al.
(HGM9) Cytogenet Cell Genet 46 : 603. 1987
8MYL4, MYL3
Chromosomal assignment of two myosin alkali light chain genes encoding the ventricular/slow skeletal muscle isoform and the atrial/foetal muscle, isoform.
Cohen-Haguenauer O, et al.
(HGM9) Cytogenet Cell Genet 46 : 595. 1987
9MYL1, MYL4, MYL3
The complete nucleotide sequences of cDNA clones coding for human myosin light chains 1 and 3.
Seidel U, et al.
Nucleic Acids Res 15 : 4989. 1987