Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness - Concepedia

Concepedia

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Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

513

Citations

26

References

1998

Year

Bech-Hansen Nt, Ben F. Koop, M. B. Mets, Musarella Ma, Boycott Km

Nature Genetics

Calcium-channel α1-Subunit GeneMolecular NeuroscienceDevelopmental BiologyOphthalmologyGenetic DisorderGeneticsFragile X SpectrumMolecular GeneticsLoss-of-function MutationsMedicine

References

	Year	Citations

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