Expansion of the Clinical Ocular Spectrum of Wolfram Syndrome in a Family Carrying a Novel WFS1 Gene Deletion

By Chacón-Camacho Oscar   Arce-Gonzalez Rocio   Granillo-Alvarez Mariella   Flores-Limas Sanjuanita   Ramírez Magdalena   Zenteno Juan C.  

Ophthalmic Genetics, Vol. 34, Iss. 4, 2013-12 ,pp. : 243-248

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Novel Mutations in MYO7A and USH2A in Usher Syndrome

By Maubaret Cécilia   Griffoin Jean-Michel   Arnaud Bernard   Hamel Christian  

Ophthalmic Genetics, Vol. 26, Iss. 1, 2005-03 ,pp. : 25-29

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Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa

By Zhao Kanxing   Wang Lejin   Wang Li   Wang Liming   Zhang Qingsheng   Wang Qing  

Ophthalmic Genetics, Vol. 22, Iss. 3, 2001-09 ,pp. : 187-194

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Screening of the USH1G Gene among Spanish Patients with Usher Syndrome. Lack of Mutations and Evidence of a Minor Role in the Pathogenesis of the Syndrome

By Aller Elena   Jaijo Teresa   Beneyto Magdalena   Nájera Carmen   Morera Constantino   Pérez-Garrigues Herminio   Ayuso Carmen   Millán Jose  

Ophthalmic Genetics, Vol. 28, Iss. 3, 2007-07 ,pp. : 151-155

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The changing face of Usher syndrome: Clinical implications

By Cohen Mazal   Bitner-Glindzicz Maria   Luxon Linda  

International Journal of Audiology, Vol. 46, Iss. 2, 2007-02 ,pp. : 82-93

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