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Sickle cell disease: papers with a genetic focus in the literature

he recent reporting in the media of one man’s gene editing treatment to reverse the effect of his sickle cell disease has thrust this condition into the limelight. The following are examples of open-access coverage of sickle cell genetics in the current literature.

Techniques for the detection of sickle cell disease: a review

Arishi WA, Alhadrami HA, Zourob M. Micromachines (Basel) 2021; 12 (5): 519. doi: 10.3390/mi12050519.

Sickle cell disease (SCD) is a widespread condition caused by a mutation in the beta-globin gene that leads to the production of abnormal haemoglobin – haemoglobin S. The inheritance of the mutation could be homozygous or heterozygous combined with another haemoglobin mutation.

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Upcoming Events

Participants’ Meeting: UK NEQAS Immunology, Immunochemistry & Allergy

Sheffield Hallam University, City Campus, Howard Street, Sheffield
24 May, 2024

Med-Tech Innovation Expo

NEC, Birmingham
5-6 June, 2024

UK NEQAS Blood Coagulation: Clinical and Laboratory Haemostasis 2024

Sheffield Hallam University
5-6 June, 2024

LabMedUK24

DoubleTree by Hilton Brighton Metropole
10-12 June, 2024

Infection Diagnostics Symposium 2024

IET Austin Court, Birmingham
26-27 June, 2024

SHOT Symposium 2024

Mercure Manchester Piccadilly Hotel
9 July, 2024

Access the latest issue of Pathology In Practice on your mobile device together with an archive of back issues.

Download the FREE Pathology In Practice app from your device's App store

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