A novel recessive GUCY2D mutation causing cone-rod dystrophy and not Leber's congenital amaurosis.

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Ugur I., DURLU Y., TOLUN A.

European journal of human genetics : EJHG, vol.18, pp.1121-6, 2010 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 18
• Publication Date: 2010
• Doi Number: 10.1038/ejhg.2010.81
• Journal Name: European journal of human genetics : EJHG
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.1121-6
• Istanbul University Affiliated: No