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Article

Novel compound heterozygous mutations in CERKL cause autosomal recessive retinitis pigmentosa in a nonconsanguineous Chinese family.

Archives of ophthalmology (Chicago, Ill. : 1960) - 1 Aug 2009

Tang Zhaohui, Wang Zhaoxiang, Wang Zhi, Ke Tie, Wang Qing Kenneth, Liu Mugen

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19667359
DOI: 10.1001/archophthalmol.2009.207

Genes

CERKL

Provenance

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Novel compound heterozygous mutations in CERKL cause autosomal recessive retinitis pigmentosa in a nonconsanguineous Chinese family.PMID 19667359Read ↗

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