← Evidence map

ArticleHernia : the journal of hernias and abdominal wall surgery2017

Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia.

E Mihailov et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

3 papers cite it

2017
2018
2019
2020
2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 27115767