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Reference Patent

Reference - List

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  • Search Condition : Filter (MeSH = Heterozygote*)
Species Resource RRC ID Title Journal Published Link
Human and Animal Cells NHSF46(RCB0162) , GM2-1TKB(RCB0697) 41525 Compound heterozygosity with two novel mutations in the HEXB gene produces adult Sandhoff disease presenting as a motor neuron disease phenotype. J Neurol Sci 2002-3-30 Pubmed Full text
Human and Animal Cells CHO-K1 37669 Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations. Clin Sci (Lond) 2009-9-21 Pubmed Full text
Mice RBRC02227 32640 Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects. Hum Mol Genet 2015-3-1 Pubmed Full text
C.intestinalis / (O.japonicus) Wild C. int 31334 Sustained heterozygosity across a self-incompatibility locus in an inbred ascidian. Mol Biol Evol 2015-1-1 Pubmed Full text
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