A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiency
Journal article published in 2020 by
Yukiko Yatsuka 
,
Yoshihito Kishita ,
Luke E. Formosa ,
Masaru Shimura ,
Fumihito Nozaki,
Tatsuya Fujii,
Kazuhiro R. Nitta ,
Akira Ohtake ,
Kei Murayama ,
Michael T. Ryan ,
Yasushi Okazaki
,
Yoshihito Kishita ,
Luke E. Formosa ,
Masaru Shimura ,
Fumihito Nozaki,
Tatsuya Fujii,
Kazuhiro R. Nitta ,
Akira Ohtake ,
Kei Murayama ,
Michael T. Ryan ,
Yasushi Okazaki
This paper is made freely available by the publisher.
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