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[Complex V deficiency].
Matsumoto H, Nishino I. Matsumoto H, et al. Nihon Rinsho. 2002 Apr;60 Suppl 4:495-8. Nihon Rinsho. 2002. PMID: 12013922 Review. Japanese. No abstract available.
The expanding clinical spectrum of mitochondrial diseases.
De Vivo DC. De Vivo DC. Brain Dev. 1993 Jan-Feb;15(1):1-22. doi: 10.1016/0387-7604(93)90002-p. Brain Dev. 1993. PMID: 8338207 Review.
This classification divides mitochondrial diseases into five categories. Primary and secondary deficiencies of carnitine are examples of a substrate transport defect. ...Two clinical syndromes predominate, one involving limb weakness, and the other primarily affecti …
This classification divides mitochondrial diseases into five categories. Primary and secondary deficiencies of carnitine are e …
MtDNA and nuclear mutations affecting oxidative phosphorylation: correlating severity of clinical defect with extent of bioenergetic compromise.
Robinson BH. Robinson BH. J Bioenerg Biomembr. 1994 Jun;26(3):311-6. doi: 10.1007/BF00763102. J Bioenerg Biomembr. 1994. PMID: 8077184 Review.
Rates of ATP synthesis were studied in cultured skin fibroblasts treated with digitonin. In fibroblasts from patients with complex I deficiency, complex IV and complex V deficiency rates of ATP synthesis were decreased below the levels found in control …
Rates of ATP synthesis were studied in cultured skin fibroblasts treated with digitonin. In fibroblasts from patients with complex I defi
[Complex V (ATP synthase) deficiency].
Nonaka I. Nonaka I. Ryoikibetsu Shokogun Shirizu. 2001;(36):142-3. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596347 Review. Japanese. No abstract available.