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J.AJHG.2009.10.013
J.AJHG.2009.10.013
http://dx.doi.org/10.1016/J.AJHG.2009.10.013
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
P356
Q35011677-5311B6EB-D568-4D5B-8A59-3E9052C4AE39
P356
J.AJHG.2009.10.013
http://dx.doi.org/10.1016/J.AJHG.2009.10.013