← Evidence map

ArticleJournal of human genetics2016

Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability.

Silvia Moncini et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

11 papers cite it

2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 26657932