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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Whole exome sequencing identifies compound heterozygous variants of CR2 gene in monozygotic twin patients with common

Adiratna Mat Ripen1, Hamidah Ghani2, Chai Teng Chear1

  • 1Primary Immunodeficiency Unit, Allergy and Immunology Research Centre, Institute for Medical Research, Ministry of Health, Kuala Lumpur, Malaysia.

SAGE Open Medicine
|June 18, 2020
PubMed
Abstract

Keywords:
Respiratory medicineallergy/immunologypaediatricprimary immunodeficiencieswhole exome sequencing

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