Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency

S Masnada, Stefan Groeneweg, V Saletti, L Chiapparini, B Castellotti, E Salsano, Edward Visser, D Tonduti

Research output: Contribution to journalArticleAcademicpeer-review

11 Citations (Scopus)
Original languageEnglish
Pages (from-to)1565-1575
Number of pages11
JournalMetabolic Brain Disease
Issue number6
Publication statusPublished - 2019

Research programs

  • EMC MM-01-39-03

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