Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans (Q24313099)
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English | Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans |
scientific article |
Statements
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans (English)
1 reference
Michel Michaelides
Genevieve A Wright
Sophie Devery
Anthony T Moore
Graham E Holder
Andrew R Webster
29 October 2009
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