Richner-Hanhart Syndrome (Tyrosine Transaminase Deficiency)
Author:
Publisher
Springer Vienna
Link
http://link.springer.com/content/pdf/10.1007/978-3-211-69500-5_42
Reference33 articles.
1. Al-Hemidan AL, al-Hazzaa SA (1995) Richner-Hanhart syndrome (Tyrosinemia type II). Case report and literature review. Ophthal Genet 16: 21–26.
2. Barr DGD, Kirk JM, Laing SC (1991) Outcome of tyrosinaemia type II. Arch Dis Child 66: 1249–1250.
3. Barton DE, Yang-Feng TL, Francke V (1986) The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22-q24) by somatic cell hybrid analysis and in situ hybridization. Hum Genet 72: 221.
4. Bonhert A, Anton-Lamprecht I (1982) Richner-Hanhart’s syndrome: ultrastructural abnormalities of epidermal keratinization indicating a causal relationship to high intracellular tyrosine levels. J Invest Dermatol 79: 68–74.
5. Burns PR (1972) The tyrosine aminotransferase deficiency: an unusual cause of corneal ulcers. Am J Opthalmol 73: 400.
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