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

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Online Access:http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.291.239
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spelling ftciteseerx:oai:CiteSeerX.psu:10.1.1.291.239 2023-05-15T16:10:23+02:00 The Pennsylvania State University CiteSeerX Archives application/zip http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.291.239 en eng http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.291.239 Metadata may be used without restrictions as long as the oai identifier remains attached to it. ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/a6/d3/Mol_Vis_2011_Jun_4_17_1485-1492.tar.gz text ftciteseerx 2016-01-07T21:34:38Z A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases Text Faroe Islands Unknown Faroe Islands
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description A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases
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