HuGE Literature Finder
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Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population. Clinical genetics 2016 May . Fattahi Zohreh, Kalhor Zahra, Fadaee Mahsa, Vazehan Raheleh, Parsimehr Elham, Abolhassani Ayda, Beheshtian Maryam, Zamani Gholamreza, Nafissi Shahriar, Nilipour Yalda, Akbari Mohammad R, Kahrizi Kimia, Kariminejad Ariana, Najmabadi Hosse |
Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes. JIMD reports 2015 23 91-100. Komulainen Tuomas, Hautakangas Milla-Riikka, Hinttala Reetta, Pakanen Salla, Vähäsarja Vesa, Lehenkari Petri, Olsen Päivi, Vieira Päivi, Saarenpää-Heikkilä Outi, Palmio Johanna, Tuominen Hannu, Kinnunen Pietari, Majamaa Kari, Rantala Heikki, Uusimaa Johan |
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- Page last updated:Mar 22, 2023
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