Molecular genetic detection of female carriers of protan defects.

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 Res

journal_title

Vision research

authors

Kainz PM,Neitz M,Neitz J

doi

10.1016/s0042-6989(97)00366-0

subject

Has Abstract

pub_date

1998-11-01 00:00:00

pages

3365-9

issue

21

eissn

0042-6989

issn

1878-5646

pii

S0042-6989(97)00366-0

journal_volume

38

pub_type

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