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A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency

Document Type

Article

Author

Lines, M.A.; Cuillerier, A.; Pileggi, C.; Harper, M.-E.; Burelle, Y.; Chakraborty, P.; Geraghty, M.T.; Naas, T.; Duque Lasio, M.L.; Toler, T.L.; Michaud, J.; Sondheimer, N.; Crawford, H.P.; Millan, F.

Source

In: European Journal of Human Genetics. (European Journal of Human Genetics, November 2021, 29(11):1719-1724)

Subject

Language

English

ISSN

14765438
10184813

Online Access

Full Text (ProQuest Central) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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