Novel compound heterozygous mutations in CERKL cause autosomal recessive retinitis pigmentosa in a nonconsanguineous Chinese family.
Novel compound heterozygous mutations in CERKL cause autosomal recessive retinitis pigmentosa in a nonconsanguineous Chinese family.
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DOI：
10.1001/archophthalmol.2009.207
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发表时间：
2009-08
影响因子：
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通讯作者：
Zhao-hui Tang;Zhaoxiang Wang;Zhi Wang;Tie Ke;Qing Kenneth Wang;Mugen Liu
中科院分区：
文献类型：
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作者：
Zhao-hui Tang;Zhaoxiang Wang;Zhi Wang;Tie Ke;Qing Kenneth Wang;Mugen Liu
