Molecular and cellular basis of ornithine δ-aminotransferase deficiency caused by the V332M mutation associated with gyrate atrophy of the choroid and retina-Reference-Cited by-同舟云学术

Molecular and cellular basis of ornithine δ-aminotransferase deficiency caused by the V332M mutation associated with gyrate atrophy of the choroid and retina

Published:2018-11 Issue:11 Volume:1864 Page:3629-3638
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Montioli Riccardo,Desbats Maria Andrea,Grottelli Silvia,Doimo Mara,Bellezza Ilaria,Borri Voltattorni Carla,Salviati Leonardo,Cellini Barbara

Funder

Telethon Foundation

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference42 articles.

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3. Ornithine aminotransferase, an important glutamate-metabolizing enzyme at the crossroads of multiple metabolic pathways;Ginguay;Biology,2017

4. Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2;Barrett;Invest. Ophthalmol. Vis. Sci.,1987

5. Factors influencing the activity of ornithine aminotransferase in isolated rat liver mitochondria;McGivan;Biochem. J.,1977

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