hCG1818432, isoform CRA_b [Homo sapiens]

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Evaluation of PRSS56 in Chinese subjects with high hyperopia or primary angle-closure glaucoma. [Mol Vis. 2013]
Evaluation of PRSS56 in Chinese subjects with high hyperopia or primary angle-closure glaucoma.
Jiang D, Yang Z, Li S, Xiao X, Jia X, Wang P, Guo X, Liu X, Zhang Q. Mol Vis. 2013; 19:2217-26. Epub 2013 Nov 7.
Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene. [Gene. 2013]
Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene.
Said MB, Chouchène E, Salem SB, Daoud K, Largueche L, Bouassida W, Benzina Z, Ayadi H, Söderkvist P, Matri L, et al. Gene. 2013 Oct 10; 528(2):288-94. Epub 2013 Jun 29.
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1. [Hum Genet. 2009]
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.
Hmani-Aifa M, Ben Salem S, Benzina Z, Bouassida W, Messaoud R, Turki K, Khairallah M, Rebaï A, Fakhfekh F, Söderkvist P, et al. Hum Genet. 2009 Oct; 126(4):575-87. Epub 2009 Jun 14.

RefSeq genomic sequence
See the genomic reference sequence for the PRSS56 gene (NG_031969.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the PRSS56 gene.

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