Long-term follow-up in cases of Alport syndrome
Author:
Affiliation:
1. Department of Otolaryngology, Head and Neck Surgery, Yamagata University Faculty of Medicine
Publisher
Japan Audiological Society
Link
https://www.jstage.jst.go.jp/article/audiology/62/4/62_299/_pdf
Reference17 articles.
1. 1) Alport AC: Hereditary familial congenital hae-morrhagic nephritis. Br Med J 1: 504-506, 1927
2. 2) Cosgrove D, Samuelson G, Meehan DT, et al: Ultrastructural, physiological, and molecular defects in the inner ear of a gene-knockout mouse model for autosomal Alport syndrome. Hear Res 121: 84-98, 1998
3. 3) Zehnder AF, Adams JC, Santi PA, et al: Distribution of type IV collagen in the cochlea in alport syndrome. Arch Otolaryngol Head Neck Surg 131: 1007-1013, 2005
4. 4) Merchant SN, Burgess BJ, Adams JC, et al: Temporal bone histopathology in alport syndrome. Laryngoscope 114: 1609-1618, 2004
5. 5) Rosado C, Bueno E, Fraile P, et al: A new mutation in the COL4A3 gene responsible for autosomal dominant Alport syndrome, which only generates hearing loss in some carriers. Eur J Med Genet 58: 35-38, 2015
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