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Entries: 1-3  
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Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy
Authors: Dadgar, Sharareh; Hagens, Olivier; Dadgar, Seyed Razi; Haghighi, Ehsan Nobakht; Schimpf, Simone; Wissinger, Bernd; Garshasbi, Masoud
Date of Publication (YYYY-MM-DD): 2006-05-12
Title of Journal: Experimental Eye Research
Volume: 83
Issue / Number: 3
Start Page: 702
End Page: 706
Document Type: Article
ID: 307521.0
 
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Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon
Authors: van den Hurk, José A. J. M.; van de Pol, Dorien J. R.; Wissinger, Bernd; van Driel, Marc A.; Hoefsloot, Lies H.; de Wijs, Ilse J.; van den Born, L. Ingeborgh; Heckenlively, John R.; Brunner, Han G.; Zrenner, Eberhart; Ropers, Hans-Hilger; Cremers, Frans P. M.
Date of Publication (YYYY-MM-DD): 2003-08
Title of Journal: Human Genetics
Volume: 113
Issue / Number: 3
Start Page: 268
End Page: 275
Document Type: Article
ID: 127646.0
Isolation of the mouse nyctalopin gene Nyx and expression studies in mouse and rat retina
Authors: Pesch, Katrin; Zeitz, Christina; Fries, Julia E.; Muenscher, Stefanie; Pusch, Carsten M.; Kohler, Konrad; Berger, Wolfgang; Wissinger, Bernd
Date of Publication (YYYY-MM-DD): 2003-05
Title of Journal: Investigative Ophthalmology & Visual Science
Volume: 44
Issue / Number: 5
Start Page: 2260
End Page: 2266
Document Type: Article
ID: 194821.0
Entries: 1-3  
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