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Cloning and characterization of the murine Vmd2 RFP-TM gene family

Krämer, F, Stöhr, H and Weber, Bernhard H. F. (2004) Cloning and characterization of the murine Vmd2 RFP-TM gene family. Cytogenetic and Genome Research 105 (1), pp. 107-114.

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Mutations in the human vitelliform macular dystrophy type 2 (VMD2) gene are known to cause autosomal dominant Best macular dystrophy (BMD), a degenerative disorder of the central retina. VMD2, together with VMD2L1, VMD2L2 and VMD2L3, belong to a closely related gene family characterized by several transmembrane (TM) spanning helical domains and an invariant arginine, phenylalanine and proline ...


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Item type:Article
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
15218265PubMed ID
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Partially
Item ID:35289
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