<scp><i>HK1</i></scp> haemolytic anaemia in association with a neurological phenotype and co‐existing <scp><i>CEP290</i> Meckel–Gruber</scp> in a Romani family

  • Erina Sasaki*
  • , Ethna Phelan
  • , Mary O'Regan
  • , Abdul Halim Kassim
  • , Jan Miletin
  • , Corrina McMahon
  • , Maureen J. O'Sullivan
  • , Julia Baptista
  • , Sally Ann Lynch
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)142-143
Number of pages0
JournalClinical Genetics
Volume101
Issue number1
Early online date16 Sept 2021
DOIs
Publication statusPublished - Jan 2022

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