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	1.	Aprataxin mutations are a rare cause of early onset ataxia in Germany. [electronic resource] by Habeck, Matthias Zühlke, Christine Bentele, Karl H P Unkelbach, Stephan Kress, Wolfram Bürk, Katrin Schwinger, Eberhard Hellenbroich, Yorck Producer: 20040923 In: Journal of neurology vol. 251 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation. [electronic resource] by Kouz, Karim Lissewski, Christina Spranger, Stephanie Mitter, Diana Riess, Angelika Lopez-Gonzalez, Vanesa Lüttgen, Sabine Aydin, Hatip von Deimling, Florian Evers, Christina Hahn, Andreas Hempel, Maja Issa, Ulrike Kahlert, Anne-Karin Lieb, Adrian Villavicencio-Lorini, Pablo Ballesta-Martinez, Maria Juliana Nampoothiri, Sheela Ovens-Raeder, Angela Puchmajerová, Alena Satanovskij, Robin Seidel, Heide Unkelbach, Stephan Zabel, Bernhard Kutsche, Kerstin Zenker, Martin Producer: 20170911 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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