(Q28301295)
Statements
Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels (English)
Jean-Charles Hoda
Francesca Zaghetto
Alexandra Koschak
1 January 2005
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Identifiers
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2 references