ArticleMetabolic brain disease2019
Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency.
Silvia Masnada et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
14 papers cite it
this papercites it
ArticleMetabolic brain disease2019
Silvia Masnada et al.PubMed ↗Publisher ↗
No numbers read from the abstract.