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A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome

✍ Scribed by Sophie Lebon; Limor Minai; Dominique Chretien; Johanna Corcos; Valérie Serre; Noman Kadhom; Julie Steffann; Jean-Yves Pauchard; Arnold Munnich; Jean-Paul Bonnefont; Agnès Rötig

Book ID: 116988016
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 197 KB
Volume: 92
Category: Article
ISSN: 1096-7192
DOI: 10.1016/j.ymgme.2007.05.010

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