By Jeffery C. Hall
ISBN-10: 012017636X
ISBN-13: 9780120176366
Advances in Genetics raises its concentrate on sleek human genetics and its relation to medication with the merger of this long-standing serial with Molecular Genetic drugs . This merger affirms theAcademic Press dedication to post very important stories of the broadest curiosity to geneticists and their colleagues in affiliated disciplines.
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5th Annu. Eur. , London, 1996. 1. , Mueller, J.. , Snipes, G. , Shooter, E. , Patel, P. I.. and Lupski, J. R. (1993a). Charcot-Marie-Tooth disease type 1A. Association with a point mutation in the PMP22 gene. Engl. J. Med. 329:96-101. , Marks, H. , Chance, P. , and Lupski, J. R. (1993h). Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene. Nat. Genet. 5 :269-27 3. , anJ Hood, L. E. (1983). Characterisation ofcloned cDNA representing rat myelin basic protein: Absence of expression in brain of shiverer mutant mice.
J. 62:172-182. Davies, D. M. ( 1954). Recurrent peripheral nerve palsies in a family. Lancet 2:266-268. 38 C. Bell and N. Hailes Dehruyne, J.. , and Martin, J . J. (1980). Hereditary pressure sensitive neuropathy. J. Neurol. Sci. 47:385-394. Defesche. 1. , Hoogendijk, J. , Ongerhoer de Visser, B. , and Bolhuis, P. A. ( 1990). Genetic linkage of hereditary motor and sensory neuropathy type 1 (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17. Neurologj 40:1450-1453. , and Sottas, J.
Mol. Genet. 3:355-358. lonasescu, V. , and Neahring, R. (1995). Dejerine-Sottas disease with de nowo dominant point mutation of the PMP22 gene. Neurology 45:1766-1767. Ionasescu, V. , and Werner, R. (1996). Mutations of the noncoding region of the connexin32 gene in X-linked Charcot-Marie-Tooth neuropathy. Neurology 46:A173 (Abstr. 010). Kirschner, D. , and Gamer, A. L. (1980). Compact myelin exists in the absence of basic protein in the shiwerer mutant mouse. Nature (London) 283:207-210. F. (1996).
Advances in Genetics, Vol. 36 by Jeffery C. Hall
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