Abstract:
:Females heterozygous for congenital colour vision defects are of interest because they are believed to have cone photoreceptor ratios and cone photopigments that differ from normal. We describe a molecular genetic method to identify protan carriers that involves characterizing the genes that occur in the most upstream position in each of the X-chromosome photopigment gene arrays.
journal_name
Vision Resjournal_title
Vision researchauthors
Kainz PM,Neitz M,Neitz Jdoi
10.1016/s0042-6989(97)00366-0subject
Has Abstractpub_date
1998-11-01 00:00:00pages
3365-9issue
21eissn
0042-6989issn
1878-5646pii
S0042-6989(97)00366-0journal_volume
38pub_type
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