Neurofibromatosis type 2 (NF2) is a rare autosomal dominant disease, characterized by the development of bilateral vestibular schwannomas. The NF2 gene has been assigned t o chromosome 22. Cataract and other eye abnormalities are frequently seen in NF2 patients. The specific association of eye abnor
✦ LIBER ✦
A Second Gene for Cerulean Cataracts Maps to the β Crystallin Region on Chromosome 22
✍ Scribed by Patricia Kramer; Jennifer Yount; Thomas Mitchell; Dante LaMorticella; Roque Carrero-Valenzuela; Everett Lovrien; Irene Maumenee; Michael Litt
- Book ID
- 115613349
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 96 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0888-7543
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