Bare Lymphocyte Syndrome 2
What's New
Last Posted: Feb 02, 2023
- A novel mutation in the TAP2 gene in bare lymphocyte syndrome: association with metastatic cutaneous squamous cell carcinoma.
España Agustín, et al. Archives of dermatology 2010 0 (1) 96-8 - Bare lymphocyte syndrome
From NCATS Genetic and Rare Diseases Information Center - Bare lymphocyte syndrome 2
From NCATS Genetic and Rare Diseases Information Center - Single nucleotide polymorphisms in the gene encoding the major histocompatibility complex class II transactivator (CIITA) in systemic lupus erythematosus.
Koizumi K, et al. Annals of the rheumatic diseases 2005 6 (6) 947-50 - Single nucleotide polymorphisms in MHC2TA, the gene encoding the MHC class II transactivator (CIITA).
Patarroyo J C, et al. Genes and immunity 2002 2 (1) 34-7
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
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- Page last reviewed:Feb 1, 2024
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