DNM1L‐related encephalopathy in infancy with Leigh syndrome‐like phenotype and suppression‐burst. Issue 5 (14th June 2016)

• Record Type: Journal Article
• Authors: Zaha, K.; Matsumoto, H.; Itoh, M.; Saitsu, H.; Kato, K.; Kato, M.; Ogata, S.; Murayama, K.; Kishita, Y.; Mizuno, Y.; Kohda, M.; Nishino, I.; Ohtake, A.; Okazaki, Y.; Matsumoto, N.; Nonoyama, S.
• Is Part Of: Clinical genetics. Volume 90:Issue 5(2016)
• Page Start: 472
• Page End: 474
• Publication Date: 2016-06-14
• Subjects: Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/cge.12805
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract :