Source: International Congress 2018 – Genetics in chronic pulmonary diseases
Disease area: Paediatric lung diseases



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A. Kassim (Kuala Lumpur, Malaysia), A. Mat Ripen (Kuala Lumpur, Malaysia), H. Ghani (Kuala Lumpur, Malaysia), C. Chear (Kuala Lumpur, Malaysia), S. Mohamad (Kuala Lumpur, Malaysia). High-Coverage Whole Exome Sequencing Identifies Novel Frameshift Deletion of LRBA Gene in Monozygotic Twin with Common Variable Immunodeficiency.. 4228

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