← Evidence map

ArticleNeurogenetics2017

Recurrent KIF2A mutations are responsible for classic lissencephaly.

Mara Cavallin et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

20 papers cite it

2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 27747449