Novel Cythochrome P4501B1 (CYP1B1) Gene Mutations in Japanese Patients with Primary Congenital Glaucoma

ERRATUM

Erratum in: “Novel Cythochrome P4501B1 (CYP1B1) Gene Mutations in Japanese Patients with Primary Congenital Glaucoma” by Mashima et al. (Invest Ophthalmol Vis Sci. 2001;42:2211–2216). 

On p. 2213, some numbers in Table 1 were transposed. The corrected table appears below, with the correct numbers in bold. 

The online version of this article was corrected on October 3, 2001. 

Table 1.

 

 

Summary of Mutations in the CYP1B1 Gene of Affected Individuals in 11 Japanese Families with Primary Congenital Glaucoma

Table 1.

 

Summary of Mutations in the CYP1B1 Gene of Affected Individuals in 11 Japanese Families with Primary Congenital Glaucoma

Number of Families	Mutation DNA Change (Predicted Effect)	Mutation DNA Change (Predicted Effect)
3	4776insAT (frameshift)	G7927A (Val364Met)
1	A4380T (Asp192Val)*
1	A4380T (Asp192Val)	G7927A (Val364Met)
1	G4793T, C4794T (Ala330Phe)	G7927A (Val364Met)
1	G7927A (Val364Met)	G8168A (Arg444Gln)
1	C4645A (Cys280stop)	G8168A (Arg444Gln)
1	3964delC (frameshift)	G8168A (Arg444Gln)
2	C3130T (unknown)†	G4763T (Val320Leu)
1	G4397A (Val198Ile)‡	Unidentified
1	A8333G (Glu499Gly)‡	Unidentified

 * Homozygous.  † Probable mutation in the noncoding region of exon 1.  ‡ Probable mutation found in one of two alleles.