نتایج جستجو برای: congenital stationary night blindness
تعداد نتایج: 223938 فیلتر نتایج به سال:
Journal:
:Investigative Opthalmology & Visual Science
2021
Journal:
:The American Journal of Human Genetics
2013
Journal:
:Journal of Clinical & Experimental Ophthalmology
2011
Journal:
:Investigative Opthalmology & Visual Science
2016
Journal:
:Russian Ophthalmological Journal
2019
Journal:
:Clinical Ophthalmology
2016
Journal:
:The Journal of neuroscience : the official journal of the Society for Neuroscience
2004
John E McRory
Jawed Hamid
Clinton J Doering
Esperanza Garcia
Robin Parker
Kevin Hamming
Lina Chen
Michael Hildebrand
Aaron M Beedle
Laura Feldcamp
Gerald W Zamponi
Terrance P Snutch
Glutamate release from rod photoreceptors is dependent on a sustained calcium influx through L-type calcium channels. Missense mutations in the CACNA1F gene in patients with incomplete X-linked congenital stationary night blindness implicate the Ca(v)1.4 calcium channel subtype. Here, we describe the functional and pharmacological properties of transiently expressed human Ca(v)1.4 calcium chann...
Journal:
:Vision Research
2008
Journal:
:Journal of Medical Genetics
1994
Journal:
:Documenta Ophthalmologica
2005
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