Molecular basis of ornithine aminotransferase defect in gyrate atrophy.

G. Inana, Y. Hotta, C. Zintz, C. Chambers, N. G. Kennaway, Richard Weleber, A. Nakajima, T. Shiono

Research output: Contribution to journalArticle

3 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)191-219
Number of pages29
JournalProgress in Clinical and Biological Research
Volume362
StatePublished - 1991
Externally publishedYes

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Molecular Sequence Data
Gyrate Atrophy
Ornithine-Oxo-Acid Transaminase
Restriction Fragment Length Polymorphisms
Amino Acid Sequence
Messenger RNA
DNA

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Inana, G., Hotta, Y., Zintz, C., Chambers, C., Kennaway, N. G., Weleber, R., ... Shiono, T. (1991). Molecular basis of ornithine aminotransferase defect in gyrate atrophy. Progress in Clinical and Biological Research, 362, 191-219.

Molecular basis of ornithine aminotransferase defect in gyrate atrophy. / Inana, G.; Hotta, Y.; Zintz, C.; Chambers, C.; Kennaway, N. G.; Weleber, Richard; Nakajima, A.; Shiono, T.

In: Progress in Clinical and Biological Research, Vol. 362, 1991, p. 191-219.

Research output: Contribution to journalArticle

Inana, G, Hotta, Y, Zintz, C, Chambers, C, Kennaway, NG, Weleber, R, Nakajima, A & Shiono, T 1991, 'Molecular basis of ornithine aminotransferase defect in gyrate atrophy.', Progress in Clinical and Biological Research, vol. 362, pp. 191-219.
Inana, G. ; Hotta, Y. ; Zintz, C. ; Chambers, C. ; Kennaway, N. G. ; Weleber, Richard ; Nakajima, A. ; Shiono, T. / Molecular basis of ornithine aminotransferase defect in gyrate atrophy. In: Progress in Clinical and Biological Research. 1991 ; Vol. 362. pp. 191-219.
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