TTN c.76327G>C ;(p.E25443Q)

Variant ID: 2-179434532-C-G

NM_001267550.1(TTN):c.76327G>C;(p.E25443Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.

International Journal Of Molecular Medicine
Salvi, Alessandro A; Giacopuzzi, Edoardo E; Bardellini, Elena E; Amadori, Francesca F; Ferrari, Lia L; De Petro, Giuseppina G; Borsani, Giuseppe G; Majorana, Alessandra A
Publication Date: 2016-11

Variant appearance in text: TTN: E25443Q
PubMed Link: 27665865
Variant Present in the following documents:
  • Main text
  • ijmm-38-05-1338.pdf
View BVdb publication page