reference/12615358

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publicationName	Visual Neuroscience
startingPage	395
bibliographicCitation	Goto-Omoto S, Hayashi T, Gekka T, Kubo A, Takeuchi T, Kitahara K. Compound heterozygous CNGA3 mutations (R436W, L633P) in a Japanese patient with congenital achromatopsia. Vis Neurosci. 2006 May;23(3-4):395–402. doi: 10.1017/s095252380623308x. PMID: 16961972.
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date	200605
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language	English
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title	Compound heterozygous CNGA3 mutations (R436W, L633P) in a Japanese patient with congenital achromatopsia
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