Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy
Coenzyme Q10 (CoQ10) deficiency has been associated with an increasing number of
clinical phenotypes. Whereas primary CoQ10 defects are related to mutations in ubiquinone …
clinical phenotypes. Whereas primary CoQ10 defects are related to mutations in ubiquinone …
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy.
S Sacconi, E Trevisson, L Salviati, S Aymé… - NEUROMUSCULAR …, 2010 - iris.univr.it
Coenzyme Q (10)(CoQ (10)) deficiency has been associated with an increasing number of
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy
S Sacconi, E Trevisson, L Salviati… - Neuromuscular …, 2010 - pubmed.ncbi.nlm.nih.gov
Coenzyme Q (10)(CoQ (10)) deficiency has been associated with an increasing number of
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
[PDF][PDF] Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy
S Sacconi, E Trevisson, L Salviati, S Aymé… - Neuromuscular …, 2010 - researchgate.net
abstract Coenzyme Q10 (CoQ10) deficiency has been associated with an increasing
number of clinical phenotypes. Whereas primary CoQ10 defects are related to mutations in …
number of clinical phenotypes. Whereas primary CoQ10 defects are related to mutations in …
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy
S Sacconi, E Trevisson, L Salviati, S Aymé… - Neuromuscular …, 2010 - nmd-journal.com
Abstract Coenzyme Q 10 (CoQ 10) deficiency has been associated with an increasing
number of clinical phenotypes. Whereas primary CoQ 10 defects are related to mutations in …
number of clinical phenotypes. Whereas primary CoQ 10 defects are related to mutations in …
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy.
S Sacconi, E Trevisson, L Salviati, S Aymé… - Neuromuscul …, 2010 - hal.science
Coenzyme Q (10)(CoQ (10)) deficiency has been associated with an increasing number of
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy
S Sacconi, E Trevisson, L Salviati, S Aymé… - NEUROMUSCULAR …, 2010 - arpi.unipi.it
Coenzyme Q (10)(CoQ (10)) deficiency has been associated with an increasing number of
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
[引用][C] Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy
S Sacconi, E Trevisson, L Salviati… - Neuromuscular …, 2010 - produccioncientifica.ucm.es
Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy.
S Sacconi, E Trevisson, L Salviati, S Aymé… - Neuromuscul …, 2010 - inria.hal.science
Coenzyme Q (10)(CoQ (10)) deficiency has been associated with an increasing number of
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
clinical phenotypes. Whereas primary CoQ (10) defects are related to mutations in …
[PDF][PDF] Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy
S Sacconi, E Trevisson, L Salviati, S Aymé… - Neuromuscular …, 2010 - academia.edu
abstract Coenzyme Q10 (CoQ10) deficiency has been associated with an increasing
number of clinical phenotypes. Whereas primary CoQ10 defects are related to mutations in …
number of clinical phenotypes. Whereas primary CoQ10 defects are related to mutations in …