← Evidence map

ArticleProceedings of the National Academy of Sciences of the United States of America1997

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains.

A K Srivastava et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

92 papers cite itlatest 60 shown

1997
…
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2026
this paperpooled itcites it
Full record →Abstract, authors, funding and every citing paper · PMID 9371801