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Paris 2018
Tuesday, 18.09.2018
Genetics in chronic pulmonary diseases
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High-Coverage Whole Exome Sequencing Identifies Novel Frameshift Deletion of LRBA Gene in Monozygotic Twin with Common Variable Immunodeficiency.
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)
Source:
International Congress 2018 – Genetics in chronic pulmonary diseases
Session:
Genetics in chronic pulmonary diseases
Session type:
Thematic Poster
Number:
4228
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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