☆ 4.5 Letter

DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst

CLINICAL GENETICS (2016)

Journal

CLINICAL GENETICS

Volume 90, Issue 5, Pages 472-474

Publisher

WILEY-BLACKWELL

DOI: 10.1111/cge.12805

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Genetics & Heredity

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