Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness - Concepedia

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Publication | Open Access

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

DOI Full Paper Access

237

Citations

23

References

2009

Year

Maria M. van Genderen, Mieke M. C. Bijveld, Y. Claassen, Ralph J. Florijn, Jillian N. Pearring, Françoise Meire, Maureen A. McCall, Frans C. C. Riemslag, Ronald G. Gregg, Arthur A. Bergen,

The American Journal of Human Genetics

Developmental BiologyOphthalmologyGenetic DisorderGeneticsMedicineCommon Cause

References

	Year	Citations

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