Functional analysis of congenital stationary night blindness type-2 CACNA1F mutations F742C, G1007R, and R1049W - Concepedia

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Functional analysis of congenital stationary night blindness type-2 CACNA1F mutations F742C, G1007R, and R1049W

42

Citations

36

References

2007

Year

Jean B. Peloquin, Renata Rehak, Clinton J. Doering, John E. McRory

Developmental BiologyMendelian DisorderOphthalmologyGenetic DisorderGeneticsMolecular GeneticsFunctional AnalysisMedicineNeurogenetics

References

	Year	Citations

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