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  1. 1.   A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat
  2. Ishida, Y.; David, V. A.; Eizirik, E.; Schaffer, A. A.; Neelam, B. A.; Roelke, M. E.; Hannah, S. S.; O'Brien, S. J.; Menotti-Raymond, M.
  3. Genomics. 2006, Dec; 88(6): 698-705.
  1. 2.   Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice
  2. Wilson, S. M.; Householder, D. B.; Coppola, V.; Tessarollo, L.; Fritzsch, B.; Lee, E. C.; Goss, D.; Carlson, G. A.; Copeland, N. G.; Jenkins, N. A.
  3. Genomics. 2001 74(2): 228-233.
  1. 3.   The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a
  2. Jones, J. M.; Huang, J. D.; Mermall, V.; Hamilton, B. A.; Mooseker, M. S.; Escayg, A.; Copeland, N. G.; Jenkins, N. A.; Meisler, M. H.
  3. Human Molecular Genetics. 2000 9(5): 821-828.
  1. 4.   Direct interaction of microtubule- and actin-based transport motors
  2. Huang, J. D.; Brady, S. T.; Richards, B. W.; Stenoien, D.; Resau, J. H.; Copeland, N. G.; Jenkins, N. A.
  3. Nature. 1999 397(6716): 267-270.
  1. 5.   Role of myosin VI in the differentiation of cochlear hair cells
  2. Self, T.; Sobe, T.; Copeland, N. G.; Jenkins, N. A.; Avraham, K. B.; Steel, K. P.
  3. Developmental Biology. 1999 214(2): 331-341.
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