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	1.	A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4. [electronic resource] by Argente-Escrig, Herminia Sánchez-Monteagudo, Ana Frasquet, Marina Millet-Sancho, Elvira Martínez-Rubio, Maria Dolores Pitarch, Inmaculada Tomás, Miguel Espinós, Carmen Lupo, Vincenzo Sevilla, Teresa Producer: 20200817 In: Journal of the neurological sciences vol. 402 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy. [electronic resource] by Moreau-Le Lan, Sarah Aller, Elena Calabria, Ines Gonzalez-Tarancon, Lola Cardona-Gay, Cristina Martinez-Matilla, Marina Aparisi, Maria J Selles, Jorge Sagath, Lydia Pitarch, Inmaculada Muelas, Nuria Cervera, Jose V Millan, Jose M Pedrola, Laia Producer: 20190507 In: PloS one vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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