Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspects-Reference-Cited by-同舟云学术

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Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspects

Published:2021-01 Issue:1 Volume:1869 Page:140555
ISSN:1570-9639
Container-title:Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics

Author:

Montioli Riccardo,Bellezza Ilaria,Desbats Maria Andrea,Borri Voltattorni Carla,Salviati Leonardo,Cellini Barbara

Funder

Telethon Foundation

Fondazione IRP Città della Speranza

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry,Biophysics,Analytical Chemistry

Reference128 articles.

1. Raised plasma-ornithine and gyrate atrophy of the choroid and retina;Simell;Lancet,1973

2. Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes;Valle;Proc. Natl. Acad. Sci. U. S. A.,1977

3. An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina;Mitchell;J. Clin. Invest.,1988

4. Retinal structure, function, and molecular pathologic features in gyrate atrophy;Sergouniotis;Ophthalmology,2012

5. Inborn errors of metabolism: gyrate atrophy;Tsang;Adv. Exp. Med. Biol.,2018

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