← Evidence map

ArticleNeurogenetics2018

Compound heterozygous mutations in two different domains of ALDH18A1 do not affect the amino acid levels in a patient with hereditary spastic paraplegia.

Maria Steenhof et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

8 papers cite it

2018
2019
2020
2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 29754261