Screening of the myelin protein zero gene in patients with Charcot-Marie-Tooth disease

Acta Biochimica Polonica

Volumn 51, Issue 1, 2004, Pages 273-280

  Nowakowski, Adam ^a,b   Kochański, Andrzej ^a  

^a MOSSAKOWSKI MEDICAL RESEARCH CENTRE   (Poland)

^b WARSAW UNIVERSITY OF LIFE SCIENCES   (Poland)

Author keywords

Charcot Marie Tooth disease; Heteroduplex analysis; MPZ gene; SSCP

Indexed keywords

MYELIN PROTEIN;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; GENE IDENTIFICATION; GENE MUTATION; GENETIC CODE; GENETIC SCREENING; HEREDITARY MOTOR SENSORY NEUROPATHY; HETERODUPLEX ANALYSIS; HUMAN; MISSENSE MUTATION; NERVE FIBER; NEUROPATHY; PROMOTER REGION; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 2342585274     PISSN: 0001527X     EISSN: None     Source Type: Journal    
DOI: 10.18388/abp.2004_3620     Document Type: Article

References (18)

1. Bird TD, Ott J, Giblett ER. (1982) Am J Hum Genet.; 34: 388-94.
2. Bort S, Nelis E, Timmerman V, Sevilla T, Cruz-Martinez F, Millan JM, Arpa J, Vilchez JJ, Prieto F, Van Broeckhoven C, Palau F. (1997) Hum Genet.; 99: 745-54.
3. Odelberg SJ, Disteche CM, Bird TD. (1993) Cell.; 72: 143-51.
4. Filbin MT, Walsh FS, Trapp BD, Pizzey JA, Tennekoon GJ. (1990) Nature.; 344: 871-2.
5. Hayasaka K, Himoro M, Sato W, Takada G, Uyemura K, Shimizu N, Bird TD, Conneal PM, Chance PF. (1993) Nat Genet.; 5: 31-4.
6. Kochanski A, Kabzińska D, Nowakowski A, Drac H, Hausmanowa-Petrusewicz I. (2004) J Periph Nerv Syst.; 9: 1-2.
7. Kochanski A, Drac H, Kabzinska D, Ryniewicz B, Rowinska-Marcinska K, Nowakowski A, Hausmanowa-Petrusewicz I. (2004) Neurology.; in press.
8. Lemke G, Lamar E, Patterson J. (1988) Neuron.; 1: 73-83.
9. Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, Martin J, Van Broeckhoven C. (1994) Hum Genet.; 94: 653-7.
10. Nelis E, Warner L, Vriendt E, Chance Ph, Lupski J, Van Broeckhoven C. (1996) Eur J Hum Genet.; 4: 329-33.
11. Marrosu HG, Vacargio S, Marrosu CS, Vanelli A, Cianchetti C, Muntoni F. (1999) Neurology.; 52: 1110-1.
12. Mersiyanova IV, Ismailov SM, Polyakov AV, Dadali EL, Fedorov VP, Nelis E, Lofgren A, Timmerman V, Van Broeckhoven C, Evgrafov OV. (2000) Hum Mutat.; 15: 340-7.
13. Roa BB, Warner LE, Garcia CA, Russo D, Lovelace R, Chance PF, Lupski JR. (1996) Hum Mutat.; 7: 36-43.
14. Raemaekers P, Timmerman V, Nelis E, De Jonghe P, Hoogendijk JE, Baas F, Barker DF, Martin JJ, de Visser M, Bolhuis PA, Van Broeckhoven C. (1991) Neuromusc Disord.; 1: 93-7.
15. Warner L, Hilz M, Appel S, Killian JM, Kolodny EH, Karpati G, Carpenter S, Watters G, Wheeler C, Witt D, Bodell A, Nelis E, Van Broeckhoven C, Lupski J. (1996) Neuron.; 17: 451-60.
16. White MB, Carvalho M, Derse D, O'Brian SJ, Dean M. (1992) Genomics.; 12: 301-6.
17. Szigeti K, Saifi GM, Armstrong D, Belmont JW, Miller G, Lupski JR. (2003) Ann Neurol.; 54: 398-402.
18. Young P, Stogbauer F, Wiebusch H, Lofgren A, Timmerman V, Broeckhoven C, Ringelstein E, Assmann G, Funke H. (1998) Neurology.; 50: 760-3.