Kenton Holden to Base Sequence
This is a "connection" page, showing publications Kenton Holden has written about Base Sequence.
Connection Strength
0.056
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Expanding CEP290 mutational spectrum in ciliopathies. Am J Med Genet A. 2009 Oct; 149A(10):2173-80.
Score: 0.018
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A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia. Am J Med Genet A. 2005 Sep 15; 138(1):70-2.
Score: 0.014
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X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. Eur J Hum Genet. 2003 Dec; 11(12):937-44.
Score: 0.012
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X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28. Am J Hum Genet. 2002 May; 70(5):1349-56.
Score: 0.011