DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.
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.
Zaha K, et al. Among authors: mizuno y.
Clin Genet. 2016 Nov;90(5):472-474. doi: 10.1111/cge.12805. Epub 2016 Jun 14.
Clin Genet. 2016.
PMID: 27301544
No abstract available.