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Pac.RE921.S7 2000 c.4
Copies In: 3
Copies Owned: 3
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TITLE: Genetic basis of total colourblindness among Pingelapese islanders / Olof H. Sundin, Jun-Ming Yang, Yingying Li, Danping Zhu, Jane N. Hurd, Thomas N. Mitchell, Eduardo D. Silva, & Irene Hussels Maumenee.
ADDED TITLE: Colourblindness among Pingelapese islanders.
AUTHOR: Sundin, Olof H.m [et. al]
SERIES: Serials articles (Pac.)
PUBLISHED: [s.l.] : Nature America Inc., 2000.
DESCRIPTION: 289-293 p. : ill. ; 28 cm.
NOTES: Photocopied from: Nature Genetics, Vol. 25, July 2000, pp. 289-293.
NOTES: Complete achromatopsia is a rare, autosomal recessive disorder characterized by photophobia, low visual acuity, nystagmus and a total inability to distinguish colours. In this disease, cone photoreceptors, the retinal sensory neurons mediating colour vision, seem viable but fail to generate an electrical response to light. Achromatopsia, or rod monochromatism, was first mapped to 2p11?2q12 (MIM 216900; ref. 3), where it is associated with missense mutations in CNGA3 (ref. 4). CNGA3 encodes the ?-subunit of the cone cyclic nucleotide-
NOTES: gated cation channel, which generates the light-A second locus at 8q21?
NOTES: q22 has been identified among the Pingelapese islanders of Micronesia, who have a high incidence of recessive achromatopsia (MIM 262300). Here we narrow the achromatopsia locus to 1.4 cM and show that Pingelapese
NOTES: evoked electrical responses of cone photoreceptors. Achromatopsia segregates with a missense mutation at a highly conserved site in CNGB3, a new gene that encodes the ?-subunit of the cone cyclic nucleotide-
NOTES: gated cation channel. Two independent frameshift deletions establish thatachromatopsia is the null phenotype of CNGB3. Combined with earlier findings,
NOTES: our results demonstrate that both ?- and ?-subunits of the cGMP-gated channel are essential for phototransduction in all three classes of cones.
SUBJECT: Color blindness--Pohnpei (Micronesia)--Pingelap Atoll.
SUBJECT: Achromatopsia--Pohnpei (Micronesia)--Pingelap Atoll.
SUBJECT: Linkage (Genetics)--Pingelap Atoll, Pohnpei.
SUBJECT: Pingelap--Micronesian people.
SUBJECT: Pingelap Atoll.
SUBJECT: Eye diseases--Pingelap Atoll.
ADDED ENTRY: Sundin, Olof H.
ADDED ENTRY: Yang, Jun-Ming
ADDED ENTRY: Li, Yingying
ADDED ENTRY: Zhu, Danping
ADDED ENTRY: Hurd, Jane N.
ADDED ENTRY: Mitchell, Thomas N.
ADDED ENTRY: Silva, Eduardo D.

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