Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT

1. Neeve, V.C.M.
2. Pyle, A.
3. Boczonadi, V.
4. Gomez-Duran, A.
5. Griffin, H.
6. Santibanez-Koref, M.
7. Gaiser, U.
8. Bauer, P.
9. Tzschach, A.
10. Chinnery, P.F.
11. Horvath, R.

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DOI: 10.1016/J.MITO.2013.03.002 GOOGLE SCHOLAR lock_openOpen access editor

Data source: Scopus