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	1.	A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle disease. [electronic resource] by Quintans, Beatriz Sanchez-Andrade, Amalia Teijeira, Susana Fernandez-Hojas, Roberto Rivas, Eloy López, María José Navarro, Carmen Producer: 20040810 In: Archives of neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Unusual clinical findings and Complex III deficiency in a family with myotonic dystrophy. [electronic resource] by Seijo-Martínez, Manuel Castro del Río, María Campos, Yolanda Palau, Francisco Arenas, Joaquín Teijeira, Susana Fernández Hojas, Roberto Navarro, Carmen Producer: 20030428 In: Journal of the neurological sciences vol. 208 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of six novel mutations in the acid alpha-glucosidase gene in three Spanish patients with infantile onset glycogen storage disease type II (Pompe disease). [electronic resource] by Fernandez-Hojas, Roberto Huie, Maryann L Navarro, Carmen Dominguez, Carmen Roig, Manuel Lopez-Coronas, Diana Teijeira, Susana Anyane-Yeboa, Kwame Hirschhorn, Rochelle Producer: 20020318 In: Neuromuscular disorders : NMD vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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