<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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