L. A. Benoit

Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy.

Ramesh, V, McClatchey, A I, Ramesh, N, Benoit, L A, Berson, E L, Shih, V E, ...

Gyrate atrophy (GA), a recessive eye disease involving progressive loss of vision due to chorioretinal degeneration, is associated with a deficiency of the mitochondrial enzyme ornithine...

Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy.

Ramesh, V, McClatchey, A I, Ramesh, N, Benoit, L A, Berson, E L, Shih, V E, ...

Gyrate atrophy (GA), a recessive eye disease involving progressive loss of vision due to chorioretinal degeneration, is associated with a deficiency of the mitochondrial enzyme ornithine...

The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy.

Ramesh, V, Benoit, L A, Crawford, P, Harvey, P T, Shows, T B, Shih, V E, ...

A cDNA probe (HOAT1) for ornithine aminotransferase (OAT) has recently been used to map (1) the structural gene for this enzyme to chromosome 10 and (2) several related DNA sequences to the X...