机译:LRP5 BIALLELIC MUTATIONS CAUSE A HIGHER INCIDENCE OF SEVERE PHENOTYPE COMPARED WITH LRP5 MONOALLELIC MUTATION
Shanghai Jiao Tong University,Shanghai Jiao Tong Univ;
autosomal recessive; binocular involvement; FEVR; LRP5; mutation; severe phenotype; FAMILIAL EXUDATIVE VITREORETINOPATHY; NORRIE DISEASE; VARIANTS; FZD4; SPECTRUM; PROBANDS; TSPAN12; NDP;