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Results 1 - 5 of 5 for "Alexander's" disease
  1. ... person inherits the mutation from one affected parent. Alexander's disease ALX AxD Demyelinogenic leukodystrophy Dysmyelinogenic leukodystrophy Fibrinoid degeneration ...
  2. ... identified more than 50 GFAP mutations that cause Alexander disease. Most of these mutations change one of the ... of myelin, causing the signs and symptoms of Alexander disease. More About This Health Condition FLJ45472 GFAP_HUMAN ...
  3. ... PubMed Giunta C, Steinmann B. Gene symbol: COL1A2. Disease: Ehlers-Danlos syndrome type VIIB. Hum Genet. 2008 Jun;123(5):540. No abstract available. Citation on PubMed Lim J, Grafe I, Alexander S, Lee B. Genetic causes and mechanisms of Osteogenesis ...
  4. ... novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) ... J, Grafe I, Alexander S, Lee B. Genetic causes and mechanisms of Osteogenesis ...
  5. ... sons. Brittle bone disease ... PubMed Lim J, Grafe I, Alexander S, Lee B. Genetic causes and mechanisms of Osteogenesis ...