Clinical manifestations of type IV collagen mutations can vary from the severe, clinically and genetically heterogeneous renal disorder, Alport syndrome, to autosomal dominant familial benign hematuria. The predominant form of Alport syndrome is X-linked; more than 160 different mutations have yet b
The clinical spectrum of homozygous HOXA1 mutations
β Scribed by Thomas M. Bosley; Ibrahim A. Alorainy; Mustafa A. Salih; Hesham M. Aldhalaan; Khaled K. Abu-Amero; Darren T. Oystreck; Max A. Tischfield; Elizabeth C. Engle; Robert P. Erickson
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 134 KB
- Volume
- 146A
- Category
- Article
- ISSN
- 1552-4825
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