Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

S Kohl, T Marx, I Giddings, H Jägle, SG Jacobson… - Nature …, 1998 - nature.com
Abstract Total colourblindness (OMIM 216900), also referred to as rod monochromacy (RM)
or complete achromatopsia, is a rare, autosomal recessive inherited and congenital disorder …
被引用次数：419 相关文章

[引用][C] Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

S Kohl, T Marx, I Giddings, H Jägle, SG Jacobson… - Nature Genetics, 1998 - cir.nii.ac.jp
Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone
photoreceptor cGMP-gated cation channel | CiNii Research CiNii 国立情報学研究所 学術情報 …

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel

S Kohl, T Marx, I Giddings, H Jägle… - Nature …, 1998 - pubmed.ncbi.nlm.nih.gov
Total colourblindness (OMIM 216900), also referred to as rod monochromacy (RM) or
complete achromatopsia, is a rare, autosomal recessive inherited and congenital disorder …

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel.

S Kohl, T Marx, I Giddings, H Jägle… - Nature …, 1998 - search.ebscohost.com
Abstract Total colourblindness (OMIM 216900), also referred to as rod monochromacy (RM)
or complete achromatopsia, is a rare, autosomal recessive inherited and congenital disorder …

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.

S Kohl, T Marx, I Giddings, H Jägle, SG Jacobson… - Nature …, 1998 - europepmc.org
Total colourblindness (OMIM 216900), also referred to as rod monochromacy (RM) or
complete achromatopsia, is a rare, autosomal recessive inherited and congenital disorder …

[引用][C] Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

S KOHL, T MARX, I GIDDINGS, H JÄGLE… - Nature …, 1998 - pascal-francis.inist.fr
Total colourblindness is caused by mutations in the gene encoding the α-subunit of the
cone photoreceptor cGMP-gated cation channel CNRS Inist Pascal-Francis CNRS Pascal …

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel.

S Kohl, T Marx, I Giddings, H Jägle… - Nature …, 1998 - search.ebscohost.com
Abstract Total colourblindness (OMIM 216900), also referred to as rod monochromacy (RM)
or complete achromatopsia, is a rare, autosomal recessive inherited and congenital disorder …

[引用][C] Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel

S KOHL - Nat Genet, 1998 - cir.nii.ac.jp
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the
cone photoreceptor cGMP-gated cation channel | CiNii Research CiNii 国立情報学研究所 …

[引用][C] Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

S KOHL, T MARX, I GIDDINGS, H JÄGLE… - Nature …, 1998 - Nature Publishing Group