Deoxyguanosine kinase mutations and combined deficiencies of the mitochondrial respiratory chain in patients with hepatic involvement.

Slama, A; Giurgea, I; Debrey, D; Bridoux, D; de Lonlay, P; Levy, P; Chretien, D; Brivet, M; Legrand, A; Rustin, P; Munnich, A; Rötig, A

Slama, A; Giurgea, I; Debrey, D; Bridoux, D; de Lonlay, P; Levy, P; Chretien, D; Brivet, M; Legrand, A; Rustin, P; Munnich, A; Rötig, A.

Affiliation

Slama A; Laboratoire de Biochimie 1, APHP, hôpital de Bicêtre, Le Kremlin-Bicêtre, France. abdel.slama@bct.aphp.fr

Mol Genet Metab ; 86(4): 462-5, 2005 Dec.

Article in En | MEDLINE | ID: mdl-16263314

Subject(s)

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Phosphotransferases (Alcohol Group Acceptor) / Mitochondrial Diseases Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male Language: En Journal: Mol Genet Metab Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Year: 2005 Document type: Article Affiliation country:

Search on Google

Add to My VHL

XML

PubMed Links