Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss. Individuals with Usher syndrome type I have profound congenital deafness, vestibular areflexia and usually begin to exhibit signs of RP in early adolescence. In the present stu
✦ LIBER ✦
Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II
✍ Scribed by Michael D. Weston; Mirjam W.J. Luijendijk; Kurt D. Humphrey; Claes Möller; William J. Kimberling
- Book ID
- 117854375
- Publisher
- American Society of Human Genetics
- Year
- 2004
- Tongue
- English
- Weight
- 594 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/381685
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