| Literature DB >> 31444685 |
Bandar Al-Saud1,2, Huda Alajlan3, Haneen Sabar4, Siddiq Anwar5, Hibah Alruwaili3, Turki Al-Hussain6, Nada Alamri5, Anas M Alazami7,8.
Abstract
Entities:
Keywords: Gitelman syndrome; MST1; NGS; Primary immunodeficiency; autosomal recessive; combined immunodeficiency diseases; infection; molecular genetics; renal
Mesh:
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Year: 2019 PMID: 31444685 DOI: 10.1007/s10875-019-00682-9
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317