Yusuke Nakamura to Pedigree
This is a "connection" page, showing publications Yusuke Nakamura has written about Pedigree.
Connection Strength
0.112
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Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues. Am J Hum Genet. 2003 Jan; 72(1):73-82.
Score: 0.042
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Submicroscopic deletions at 13q32.1 cause congenital microcoria. Am J Hum Genet. 2015 Apr 02; 96(4):631-9.
Score: 0.024
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Aberrant splicing caused by a MLH1 splice donor site mutation found in a young Japanese patient with Lynch syndrome. Fam Cancer. 2012 Dec; 11(4):559-64.
Score: 0.021
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Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion. Nat Genet. 2007 Jun; 39(6):776-80.
Score: 0.014
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Heterozygous TGFBR2 mutations in Marfan syndrome. Nat Genet. 2004 Aug; 36(8):855-60.
Score: 0.012