Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation
CM Quinzii, AG Kattah, A Naini, HO Akman… - Neurology, 2005 - AAN Enterprises
Primary muscle coenzyme Q10 (CoQ10) deficiency is an apparently autosomal recessive
condition with heterogeneous clinical presentations. Patients with these disorders improve …
condition with heterogeneous clinical presentations. Patients with these disorders improve …
[引用][C] Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation
CM QUINZII, AG KATTAH, A NAINI, HO AKMAN… - …, 2005 - pascal-francis.inist.fr
Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation CNRS
Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …
Inist Pascal-Francis CNRS Pascal and Francis Bibliographic Databases Simple search …
Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation
CM Quinzii, AG Kattah, A Naini, HO Akman… - …, 2005 - pubmed.ncbi.nlm.nih.gov
Primary muscle coenzyme Q10 (CoQ10) deficiency is an apparently autosomal recessive
condition with heterogeneous clinical presentations. Patients with these disorders improve …
condition with heterogeneous clinical presentations. Patients with these disorders improve …
Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation.
CM Quinzii, AG Kattah, A Naini, HO Akman, VK Mootha… - Neurology, 2005 - europepmc.org
Primary muscle coenzyme Q10 (CoQ10) deficiency is an apparently autosomal recessive
condition with heterogeneous clinical presentations. Patients with these disorders improve …
condition with heterogeneous clinical presentations. Patients with these disorders improve …