Homo sapiens cDNA, FLJ92162, highly similar to Homo sapiens troponin I - Nucleotide

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Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease. [Sci Transl Med. 2024]
Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease.
Donkervoort S, van de Locht M, Ronchi D, Reunert J, McLean CA, Zaki M, Orbach R, de Winter JM, Conijn S, Hoomoedt D, et al. Sci Transl Med. 2024 Apr 3; 16(741):eadg2841. Epub 2024 Apr 3.
Elevation of fast but not slow troponin I in the circulation of patients with Becker and Duchenne muscular dystrophy. [Muscle Nerve. 2021]
Elevation of fast but not slow troponin I in the circulation of patients with Becker and Duchenne muscular dystrophy.
Barthel BL, Cox D, Barbieri M, Ziemba M, Straub V, Hoffman EP, Russell AJ. Muscle Nerve. 2021 Jul; 64(1):43-49.
Postoperative troponin increases after noncardiac surgery are associated with raised neurofilament light: a prospective observational cohort study. [Br J Anaesth. 2021]
Postoperative troponin increases after noncardiac surgery are associated with raised neurofilament light: a prospective observational cohort study.
Sanders RD, Craigova L, Schessler B, Casey C, White M, Parker M, Kunkel D, Blennow K, Zetterberg H, Pearce RA, et al. Br J Anaesth. 2021 Apr; 126(4):791-798. Epub 2020 Nov 4.

Homo sapiens cDNA, FLJ92162, highly similar to Homo sapiens troponin I, skeletal...
Homo sapiens cDNA, FLJ92162, highly similar to Homo sapiens troponin I, skeletal, slow (TNNI1), mRNA
gi|164698027|dbj|AK311896.1|

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Nucleotide