Gao, Mol Vis 1998; 4:16. Table 1.

Table 1 of Gao, Mol Vis 4:16, 1998.

Table 1. Diagnoses of patients screened for mutations in GNB3 and GNGT2

GNB3 - 164 patients                    GNGT2 - 148 patients

Autosomal dominant              35     Autosomal dominant              35
  CRD                           24       CRD                           22
  CD                             6       CD                             9
  MD (S/FF - 0)                  5       MD (S/FF - 1)                  4

Autosomal recessive/multiplex   37     Autosomal recessive/multiplex   38
  CRD                           29       CRD                           29
  CD                             2       CD                             1
  MD (S/FF - 3)                  6       MD (S/FF - 5)                  8

Simplex                         92     Simplex                         75
  CRD                           58       CRD                           46
  CD                            18       CD                            18
  MD (S/FF - 11)                16       MD (S/FF - 9)                 11

The number of patients in the MD category with the diagnosis of Stargardt disease/fundus flavimaculatus (S/FF) are shown in parentheses. Table abbreviations: Cone-rod dystrophy (CRD), Cone dystrophy (CD), Macular dystrophy (MD).

Gao, Mol Vis 1998; 4:16 <http://www.molvis.org/molvis/v4/p16>