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X-linked Charcot-Marie-Tooth Disease and Connexin32.
Fischbeck KH, Abel A, Lin GS, Scherer SS. Fischbeck KH, et al. Among authors: abel a. Ann N Y Acad Sci. 1999 Oct;883(1):36-41. doi: 10.1111/j.1749-6632.1999.tb08564.x. Ann N Y Acad Sci. 1999. PMID: 29086942
X-linked Charcot-Marie-Tooth disease and connexin32.
Fischbeck KH, Abel A, Lin GS, Scherer SS. Fischbeck KH, et al. Among authors: abel a. Ann N Y Acad Sci. 1999 Sep 14;883:36-41. Ann N Y Acad Sci. 1999. PMID: 10586227 Review.
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.
Antonellis A, Ellsworth RE, Sambuughin N, Puls I, Abel A, Lee-Lin SQ, Jordanova A, Kremensky I, Christodoulou K, Middleton LT, Sivakumar K, Ionasescu V, Funalot B, Vance JM, Goldfarb LG, Fischbeck KH, Green ED. Antonellis A, et al. Among authors: abel a. Am J Hum Genet. 2003 May;72(5):1293-9. doi: 10.1086/375039. Epub 2003 Apr 10. Am J Hum Genet. 2003. PMID: 12690580 Free PMC article.
Androgen receptor mutation in Kennedy's disease.
Fischbeck KH, Lieberman A, Bailey CK, Abel A, Merry DE. Fischbeck KH, et al. Among authors: abel a. Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):1075-8. doi: 10.1098/rstb.1999.0461. Philos Trans R Soc Lond B Biol Sci. 1999. PMID: 10434308 Free PMC article. Review.
DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4).
Chen YZ, Bennett CL, Huynh HM, Blair IP, Puls I, Irobi J, Dierick I, Abel A, Kennerson ML, Rabin BA, Nicholson GA, Auer-Grumbach M, Wagner K, De Jonghe P, Griffin JW, Fischbeck KH, Timmerman V, Cornblath DR, Chance PF. Chen YZ, et al. Among authors: abel a. Am J Hum Genet. 2004 Jun;74(6):1128-35. doi: 10.1086/421054. Epub 2004 Apr 21. Am J Hum Genet. 2004. PMID: 15106121 Free PMC article.
233 results