RUI CHEN to Amino Acid Sequence
This is a "connection" page, showing publications RUI CHEN has written about Amino Acid Sequence.
Connection Strength
0.207
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Mutations in human IFT140 cause non-syndromic retinal degeneration. Hum Genet. 2015 Oct; 134(10):1069-78.
Score: 0.090
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Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing. J Med Genet. 2013 Oct; 50(10):674-88.
Score: 0.078
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Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia. J Transl Med. 2015 Jun 04; 13:179.
Score: 0.022
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Analysis of the human endogenous coregulator complexome. Cell. 2011 May 27; 145(5):787-99.
Score: 0.017