Molecular pathogenesis of achromatopsia associated with mutations in the cone cyclic nucleotide-gated channel CNGA3 subunit
about
A cyclic nucleotide-gated channel mutation associated with canine daylight blindness provides insight into a role for the S2 segment tri-Asp motif in channel biogenesis.Inactivation of TRPM2 channels by extracellular divalent copper.Whole exome sequencing unveils a frameshift mutation in CNGB3 for cone dystrophy: A case report of an Indian family.
P2860
Molecular pathogenesis of achromatopsia associated with mutations in the cone cyclic nucleotide-gated channel CNGA3 subunit
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
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2010年论文
@zh-cn
name
Molecular pathogenesis of achr ...... de-gated channel CNGA3 subunit
@ast
Molecular pathogenesis of achr ...... de-gated channel CNGA3 subunit
@en
type
label
Molecular pathogenesis of achr ...... de-gated channel CNGA3 subunit
@ast
Molecular pathogenesis of achr ...... de-gated channel CNGA3 subunit
@en
prefLabel
Molecular pathogenesis of achr ...... de-gated channel CNGA3 subunit
@ast
Molecular pathogenesis of achr ...... de-gated channel CNGA3 subunit
@en
P2093
P2860
P1476
Molecular pathogenesis of achr ...... de-gated channel CNGA3 subunit
@en
P2093
Alexander B Quiambao
Anna P Malykhina
Cynthia S Harry
J Browning Fitzgerald
Xi-Qin Ding
P2860
P304
P356
10.1007/978-1-4419-1399-9_28
P407
P577
2010-01-01T00:00:00Z