Abstract
The availability of cloned human DNA sequences combined with classic methods of genetic linkage analysis allows us to establish whether a mutation in a given gene produces an inherited disease state. In this chapter, we will describe how cloned DNA probes corresponding to the human gene for β-nerve growth factor (βNGF) can be used to determine whether an alteration in the structure or expression of this gene is the primary defect in the inherited neurological disease familial dysautonomia. Our preliminary findings are also presented.
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Breakefield, X.O., Castiglione, C.M., Coussens, L.M., Axelrod, F.B., Ullrich, A. (1984). Linkage Analysis in Familial Dysautonomia Using Variations in DNA Sequence in the β-Nerve Growth Factor Gene Region: A Beginning. In: Black, I.B. (eds) Cellular and Molecular Biology of Neuronal Development. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2717-2_20
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DOI: https://doi.org/10.1007/978-1-4613-2717-2_20
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