Immunoglobulin A Deficiency 2
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Last Posted: Dec 31, 2024
- Primary ovarian insufficiency consequence of autoimmune diseases: a bidirectional two-sample Mendelian randomization study.
Yongming Du, et al. Frontiers in endocrinology 2024 0 1417896 - Causative mechanisms and clinical impact of immunoglobulin deficiencies in Ataxia Telangiectasia.
Sanami Takada, et al. The Journal of allergy and clinical immunology 2024 0 - Genomic association and further characterisation of faecal immunoglobulin A deficiency in German Shepherd dogs.
Grützner Niels, et al. Veterinary medicine and science 2021 0 (6) 2144-2155 - Low-Risk Human Leukocyte Antigen Genes and Mild Villous Atrophy Typify Celiac Disease With Immunoglobulin A Deficiency.
Schirru Enrico, et al. Journal of pediatric gastroenterology and nutrition 2021 0 (6) 889-893 - STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency.
Lim Che Kang, et al. Frontiers in genetics 2022 0 736235 - [Study on immunoglobulin A Deficiency(IgAD) in Chinese Shanghai Blood Donors].
Lu Ping, et al. Zhongguo shi yan xue ye xue za zhi 2016 8 (4) 1216-20 - Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.
Bronson Paola G, et al. Nature genetics 2016 11 (11) 1425-1429 - Monogenic mutations associated with IgA deficiency.
Abolhassani Hassan, et al. Expert review of clinical immunology 2016 6 - Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.
Borte Stephan, et al. Blood 2012 3 (11) 2552-5 - Immunoglobulin A deficiency 2
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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