X-linked Sideroblastic Anemia
What's New
Last Posted: Jun 07, 2016
- Sideroblastic anemia: functional study of two novel missense mutations in ALAS2.
Méndez Manuel, et al. Molecular genetics & genomic medicine 2016 5 (3) 273-82 - Delta-aminolevulinate synthase 2 polymorphism is associated with maximal oxygen uptake after Living-high exercise-high training-low in a male Chinese population.
Xu Yali, et al. International journal of clinical and experimental medicine 2015 0 (11) 21617-22 - X-linked sideroblastic anemia
From NCATS Genetic and Rare Diseases Information Center
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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