TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations - Concepedia

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TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations

DOI Full Paper Access

21

Citations

23

References

2019

Year

Alaa AlTalbishi, Lina Zelinger, Christina Zeitz, Karen Hendler, Prasanthi Namburi, Isabelle Audo, Ruth Sheffer, Claudia Yahalom, Samer Khateb, Eyal Banin,

Scientific Reports

References

	Year	Citations

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