Lupski, J. R., Gonzaga-Jauregui, C., Yang, Y., Bainbridge, M. N., Jhangiani, S., Buhay, C. J., . . . Gibbs, R. A. (2013). Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy. BioMed Central.
Stile di citazione ChicagoLupski, James R., et al. Exome Sequencing Resolves Apparent Incidental Findings and Reveals Further Complexity of SH3TC2 Variant Alleles Causing Charcot-Marie-Tooth Neuropathy. BioMed Central, 2013.
Citazione MLALupski, James R., et al. Exome Sequencing Resolves Apparent Incidental Findings and Reveals Further Complexity of SH3TC2 Variant Alleles Causing Charcot-Marie-Tooth Neuropathy. BioMed Central, 2013.
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