Original language | English |
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Pages (from-to) | 142-143 |
Number of pages | 0 |
Journal | Clinical Genetics |
Volume | 101 |
Issue number | 1 |
Early online date | 16 Sept 2021 |
DOIs | |
Publication status | Published - Jan 2022 |
<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 journal › Article › peer-review