Informazioni sul sito:

Nome del dominio - csnb.it

Titolo del sito - home

Vai al sito web - home

Posizione GEO del sito

Posizione Paese - Italy

Città/Paese - Arezzo

Fornitore - Aruba S.p.A.

Site Logo

indirizzo IP:

31.11.35.155

Server dei nomi di dominio:

dns.technorail.com dns4.arubadns.cz dns2.technorail.com dns3.arubadns.net

Tutti i record:

☆ csnb.it. 3600 IN A 31.11.35.155
☆ csnb.it. 3600 IN TXT "v=spf1 include:_spf.aruba.it ~all"
☆ csnb.it. 3600 IN MX 10 mx.csnb.it.
☆ csnb.it. 3600 IN NS dns3.arubadns.net.
☆ csnb.it. 3600 IN NS dns4.arubadns.cz.
☆ csnb.it. 3600 IN NS dns2.technorail.com.
☆ csnb.it. 3600 IN NS dns.technorail.com.
☆ csnb.it. 3600 IN SOA dns.technorail.com. hostmaster.csnb.it. 2024032001 86400 7200 2592000 3600

Brief facts about csnb:

X-linked congenital stationary night blindness is a rare X-linked non-progressive retinal disorder. It has two forms, complete, also known as type-1, and incomplete, also known as type-2, depending on severity. In the complete form, there is no measurable rod cell response to light, whereas this response is measurable in the incomplete form. Patients with this disorder have difficulty adapting to low light situations due to impaired photoreceptor transmission. These patients also often have reduced visual acuity, myopia, nystagmus and strabismus. CSNB1 is caused by mutations in the gene NYX, which encodes a protein involved in retinal synapse formation or synaptic transmission. CSNB2 is caused by mutations in the gene CACNA1F, which encodes a voltage-gated calcium channel CaV1.4.

Channelopathies

Diseases of the eye and adnexa