← Evidence map

ArticleAmerican journal of human genetics2015

De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay.

Jessica X Chong et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

85 papers cite itlatest 60 shown

2015
…
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 25683120