fig4

Autosomal dominant tibial muscular dystrophy in Estonia

Figure 4. Illustration of the FINmaj variant using IGV. The FINmaj variant is an 11-bp insertion/deletion at positions chr2:179,391,923-179,391,935 (GRCh37) in exon 364 of TTN (2q31.2) and is displayed as four different sequence changes.

Journal of Translational Genetics and Genomics
ISSN 2578-5281 (Online)
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