Missense mutations in SLC25A1 are associated with congenital myasthenic syndrome type 23

Amna Al-Futaisi, Faraz Ahmad, Ghalia Al-Kasbi, Khalid Al-Thihli, Roshan Koul, Almundher Al-Maawali*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)
Original languageEnglish
Pages (from-to)666-667
Number of pages2
JournalClinical Genetics
Issue number4
Publication statusPublished - Jan 2020

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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