<scp>HK1</scp> haemolytic anaemia in association with a neurological phenotype and co‐existing <scp>CEP290 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

doi:10.1111/cge.14058

<scp>HK1</scp> haemolytic anaemia in association with a neurological phenotype and co‐existing <scp>CEP290 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

Peninsula Medical School

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	142-143
Number of pages	0
Journal	Clinical Genetics
Volume	101
Issue number	1
Early online date	16 Sept 2021
DOIs	https://doi.org/10.1111/cge.14058
Publication status	Published - Jan 2022

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10.1111/cge.14058

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@article{b11b56f059704df38184833ada5d2de1,

title = "HK1 haemolytic anaemia in association with a neurological phenotype and co‐existing CEP290 Meckel–Gruber in a Romani family",

author = "Erina Sasaki and Ethna Phelan and Mary O'Regan and Kassim, \{Abdul Halim\} and Jan Miletin and Corrina McMahon and O'Sullivan, \{Maureen J.\} and Julia Baptista and Lynch, \{Sally Ann\}",

year = "2022",

month = jan,

doi = "10.1111/cge.14058",

language = "English",

volume = "101",

pages = "142--143",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "1",

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TY - JOUR

T1 - HK1 haemolytic anaemia in association with a neurological phenotype and co‐existing CEP290 Meckel–Gruber in a Romani family

AU - Sasaki, Erina

AU - Phelan, Ethna

AU - O'Regan, Mary

AU - Kassim, Abdul Halim

AU - Miletin, Jan

AU - McMahon, Corrina

AU - O'Sullivan, Maureen J.

AU - Baptista, Julia

AU - Lynch, Sally Ann

PY - 2022/1

Y1 - 2022/1

U2 - 10.1111/cge.14058

DO - 10.1111/cge.14058

M3 - Article

SN - 0009-9163

VL - 101

SP - 142

EP - 143

JO - Clinical Genetics

JF - Clinical Genetics

IS - 1

ER -

<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

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Cite this