Gene: [0Xp1123/OATL1] ornithine aminotransferase-like 1;
|
FAG |
A coding gene related with hyperonithinemia and retinal atrophy is located in Chr 10 (see GEM:10q26/OAT)." |
|
REF |
PRO,LOC,FAG "Barrett DJ &: Invest Ophthal Vis Sci, 28, 1037-1041, 1987 MAP "Chand A &: Genomics, 30, 545-552, 1995 PRO,LOC,FAG "Lafreniere RG &: Genomics, 10, 276-279, 1991 LIN,MAP "Lafreniere RG &: CCG, 51, (HGM10), 1028, 1989 LIN,MAP "Mahtani &: CCG, 51, (HGM10), 1038, 1989 PRO,LOC,FAG "Mitchell &: AJHG, 39, A163, 1986 PRO,LOC,FAG "Ramesh &: Hum Genet, 76, 121-126, 1986 PRO,LOC,FAG "see also GEM:10q26/OAT |
|
KEY |
mito, eye, neu, mtbd |
|
CLA |
psi, basic |
|
LOC |
0X p11.23 |
|
MIM |
MIM: 311240 |
