HK1 haemolytic anaemia in association with a neurological phenotype and co‐existing CEP290 Meckel–Gruber in a Romani family
Journal article published in 2021 by
Erina Sasaki 
,
Ethna Phelan,
Mary O'Regan,
Abdul Halim Kassim,
Jan Miletin,
Corrina McMahon,
Maureen J. O'Sullivan,
Julia Baptista ,
Sally Ann Lynch
,
Ethna Phelan,
Mary O'Regan,
Abdul Halim Kassim,
Jan Miletin,
Corrina McMahon,
Maureen J. O'Sullivan,
Julia Baptista ,
Sally Ann Lynch
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