A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

Authors:	Kym Boycott Tracy Maybaum Margaret Naylor Richard Weleber Johane Robitaille Yozo Miyake Arthur Bergen Mary Pierpont William Pearce N Bech-Hansen

Institution:	Department of Medical Genetics, University of Calgary, AB, Canada.

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