- O-methyltransferase (TOMT) is a
protein encoded by the
LRTOMT gene in humans.
Located on
chromosome 11,
mutations in
LRTOMT are ****ociated with the DFNB63 form of autosomal...
- CCDC50, DIAPH1, DSPP, ESRRB, GJB3, GRHL2, GRXCR1, HGF, LHFPL5, LOXHD1,
LRTOMT, MARVELD2, MIR96, MYH14, MYH9, MYO1A, MYO3A, OTOA, PJVK, POU4F3, PRPS1,...
-
autosomal recessive 6; 600971; TMIE Deafness,
autosomal recessive 63; 611451;
LRTOMT Deafness,
autosomal recessive 67; 610265; LHFPL5 Deafness,
autosomal recessive...
