Novel HADHB mutations in a patient with mitochondrial...

Human Genome Variation 2020 / 12 Vol. 7; Iss. 1

Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiency

Nakama, Mina, Sasai, Hideo, Kubota, Mitsuru, Hasegawa, Yuki, Fujiki, Ryoji, Okuyama, Torayuki, Ohara, Osamu, Fukao, Toshiyuki
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Volume:
7
Journal:
Human Genome Variation
DOI:
10.1038/s41439-020-0097-z
Date:
December, 2020
File:
PDF, 787 KB
2020
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