A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases

Elsebet Ostergaard, Morten Duno, Mustafa Batbayli, Kaj Vilhelmsen, Thomas Rosenberg

50 Citationer (Scopus)

Abstract

The aim of the study was to elucidate the genetic background of retinitis pigmentosa (RP) in a Faroe Islands population, a genetic isolate in the North Atlantic Ocean.
OriginalsprogEngelsk
TidsskriftMolecular Vision
Vol/bind17
Sider (fra-til)1485-92
Antal sider8
ISSN1090-0535
StatusUdgivet - 2011

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