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	1.	Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reports. [electronic resource] by Kloth, Katja Synofzik, Matthis Kernstock, Christoph Schimpf-Linzenbold, Simone Schuettauf, Frank Neu, Axel Wissinger, Bernd Weisschuh, Nicole Producer: 20190930 In: BMC medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Allelic Expression Imbalance in the Human Retinal Transcriptome and Potential Impact on Inherited Retinal Diseases. [electronic resource] by Llavona, Pablo Pinelli, Michele Mutarelli, Margherita Marwah, Veer Singh Schimpf-Linzenbold, Simone Thaler, Sebastian Yoeruek, Efdal Vetter, Jan Kohl, Susanne Wissinger, Bernd Publication details: Genes Oct 2017 In: Genes vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel heterozygous OPA3 mutation located in the mitochondrial target sequence results in altered steady-state levels and fragmented mitochondrial network. [electronic resource] by Grau, Tanja Burbulla, Lena F Engl, Gertraud Delettre, Cécile Delprat, Benjamin Oexle, Konrad Leo-Kottler, Beate Roscioli, Tony Krüger, Rejko Rapaport, Doron Wissinger, Bernd Schimpf-Linzenbold, Simone Producer: 20140603 In: Journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)