← Evidence map

ArticleEuropean journal of pediatrics2015

Three cases with L1 syndrome and two novel mutations in the L1CAM gene.

Rosario Marín et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

8 papers cite it

2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 25948108