Blue cone monochromacy: Causative mutations and associated phenotypes

PURPOSE: To perform a phenotypic assessment of members of three British families with blue cone monochromatism (BCM), and to determine the underlying molecular genetic basis of disease. METHODS: Affected members of three British families with BCM were examined clinically and underwent detailed elect...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: Gardner, Jessica C., Michaelides, Michel, Holder, Graham E., Kanuga, Naheed, Webb, Tom R., Mollon, John D., Moore, Anthony T., Hardcastle, Alison J.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Molecular Vision 2009
Onderwerpen:
Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2676201/
https://ncbi.nlm.nih.gov/pubmed/19421413
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items