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Volumn 37, Issue 4, 2006, Pages 407-410

Genetic heterogeneity of day blindness in Alaskan Malamutes

Author keywords

Canine; CNGB3; Cone degeneration; Day blindness; Malamute

Indexed keywords

CYCLIC NUCLEOTIDE GATED ION CHANNELS; CYCLIC-NUCLEOTIDE GATED ION CHANNELS; ION CHANNEL;

EID: 33746256021     PISSN: 02689146     EISSN: 13652052     Source Type: Journal    
DOI: 10.1111/j.1365-2052.2006.01484.x     Document Type: Article
Times cited : (14)

References (14)
  • 1
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    • Diagnosis and differentiation of retinal disease in small animals by electroretinography
    • Acland G.M. (1988) Diagnosis and differentiation of retinal disease in small animals by electroretinography. Seminars in Veterinary Medicine and Surgery (Small Animals) 3, 15-27.
    • (1988) Seminars in Veterinary Medicine and Surgery (Small Animals) , vol.3 , pp. 15-27
    • Acland, G.M.1
  • 4
    • 0038305558 scopus 로고    scopus 로고
    • Day-blindness in three dogs: Clinical and electroretinographic findings
    • Hurn S.D., Hardman C. & Stanley R.G. (2003) Day-blindness in three dogs: clinical and electroretinographic findings. Veterinary Ophthalmology 6, 127-30.
    • (2003) Veterinary Ophthalmology , vol.6 , pp. 127-130
    • Hurn, S.D.1    Hardman, C.2    Stanley, R.G.3
  • 5
    • 0034284696 scopus 로고    scopus 로고
    • Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21
    • Kohl S., Baumann B., Broghammer M. et al. (2000) Mutations in the CNGB3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21. Human Molecular Genetics 9, 2107-16.
    • (2000) Human Molecular Genetics , vol.9 , pp. 2107-2116
    • Kohl, S.1    Baumann, B.2    Broghammer, M.3
  • 6
    • 20144382218 scopus 로고    scopus 로고
    • CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
    • Kohl S., Varsanyi B., Antunes G.A. et al. (2005) CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia. European Journal of Human Genetics 13, 302-8.
    • (2005) European Journal of Human Genetics , vol.13 , pp. 302-308
    • Kohl, S.1    Varsanyi, B.2    Antunes, G.A.3
  • 8
    • 0036801880 scopus 로고    scopus 로고
    • A frameshift insertion in the cone cyclic nucleotide gated cation channel causes complete achromatopsia in a cosanguineous family from a rural isolate
    • Rojas C.V., Santa Marìa L., Santos J.L., Cortés F. & Alliende M.A. (2002) A frameshift insertion in the cone cyclic nucleotide gated cation channel causes complete achromatopsia in a cosanguineous family from a rural isolate. European Journal of Human Genetics 10, 638-42.
    • (2002) European Journal of Human Genetics , vol.10 , pp. 638-642
    • Rojas, C.V.1    Santa Marìa, L.2    Santos, J.L.3    Cortés, F.4    Alliende, M.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.