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Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy
Journal article   Open access  Peer reviewed

Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy

G INANA, C CHAMBERS, Y HOTTA, L INOUYE, D FILPULA, S PULFORD and T SHIONO
The Journal of biological chemistry, Vol.264(29), pp.17432-17436
1989
PMID: 2793865

Abstract

Neurology Biological and medical sciences Medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
url
https://doi.org/10.1016/S0021-9258(18)71513-5View
Published (Version of record) Open

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.197 Molecular & Cell Biology - Mitochondria
1.197.1797 Ornithine Transcarbamylase Deficiency
Web Of Science research areas
Biochemistry & Molecular Biology
ESI research areas
Biology & Biochemistry

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#3 Good Health and Well-Being

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