Edinburgh Research Explorer

An Indian child with Coats plus syndrome likely due to mutations in STN1

Research output: Contribution to journalArticle

  • Gouri Rao Passi
  • Uzma Shamim
  • Aradhana Mathur
  • Shaista Parveen
  • Pooja Sharma
  • Yanick Crow
  • Mohammed Faruq

Related Edinburgh Organisations

Original languageEnglish
JournalAmerican Journal of Medical Genetics
Early online date6 Jul 2020
Publication statusE-pub ahead of print - 6 Jul 2020

ID: 148462708