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Connexin mutations in X-linked Charcot-Marie-Tooth disease.
Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, Paul DL, Chen K, Lensch MW, Chance PF, Fischbeck KH. Bergoffen J, et al. Among authors: bone lj. Science. 1993 Dec 24;262(5142):2039-42. doi: 10.1126/science.8266101. Science. 1993. PMID: 8266101
Connexin32 and X-linked Charcot-Marie-Tooth disease.
Fischbeck KH, Deschênes SM, Bone LJ, Scherer SS. Fischbeck KH, et al. Among authors: bone lj. Cold Spring Harb Symp Quant Biol. 1996;61:673-7. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246493 Review. No abstract available.
Connexin32 and X-linked Charcot-Marie-Tooth disease.
Bone LJ, Deschênes SM, Balice-Gordon RJ, Fischbeck KH, Scherer SS. Bone LJ, et al. Neurobiol Dis. 1997;4(3-4):221-30. doi: 10.1006/nbdi.1997.0152. Neurobiol Dis. 1997. PMID: 9361298 Free article. Review.
Functional gap junctions in the schwann cell myelin sheath.
Balice-Gordon RJ, Bone LJ, Scherer SS. Balice-Gordon RJ, et al. Among authors: bone lj. J Cell Biol. 1998 Aug 24;142(4):1095-104. doi: 10.1083/jcb.142.4.1095. J Cell Biol. 1998. PMID: 9722620 Free PMC article.
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome.
Muenke M, Bone LJ, Mitchell HF, Hart I, Walton K, Hall-Johnson K, Ippel EF, Dietz-Band J, Kvaløy K, Fan CM, et al. Muenke M, et al. Among authors: bone lj. Am J Hum Genet. 1995 Nov;57(5):1074-9. Am J Hum Genet. 1995. PMID: 7485157 Free PMC article.
13 results