Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Abnormalities and CAPN3[original query] |
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Respiratory chain deficiency in nonmitochondrial disease. Neurology. Genetics 2015 Jun 1 (1): e6. Pyle Angela, Nightingale Helen J, Griffin Helen, Abicht Angela, Kirschner Janbernd, Baric Ivo, Cuk Mario, Douroudis Konstantinos, Feder Lea, Kratz Markus, Czermin Birgit, Kleinle Stephanie, Santibanez-Koref Mauro, Karcagi Veronika, Holinski-Feder Elke, Chinnery Patrick F, Horvath Ri |
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients. Clinical genetics 2019 3 96 (2): 126-133. Ten Dam Leroy, Frankhuizen Wendy S, Linssen Wim H J P, Straathof Chiara S, Niks Erik H, Faber Karin, Fock Annemarie, Kuks Jan B, Brusse Esther, de Coo René, Voermans Nicol, Verrips Aad, Hoogendijk Jessica E, van der Pol Ludo, Westra Dineke, de Visser Marianne, van der Kooi Anneke J, Ginjaar Ie |
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