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Clinical expression of Duchenne and Becker muscular dystrophy with respect to manifestation in the area of Xp21.2 - locus which codifies dystrophin synthesis

Silvija Pušeljić
Vesna Milas
Mirna Sipl
Ivo Pušeljić

Puni tekst: engleski, pdf (2 MB) str. 41-44 preuzimanja: 512* citiraj
APA 6th Edition
Pušeljić, S., Milas, V., Sipl, M. i Pušeljić, I. (2002). Clinical expression of Duchenne and Becker muscular dystrophy with respect to manifestation in the area of Xp21.2 - locus which codifies dystrophin synthesis. Medicinski vjesnik, 34/35 ((1-4)), 41-44. Preuzeto s https://hrcak.srce.hr/190678
MLA 8th Edition
Pušeljić, Silvija, et al. "Clinical expression of Duchenne and Becker muscular dystrophy with respect to manifestation in the area of Xp21.2 - locus which codifies dystrophin synthesis." Medicinski vjesnik, vol. 34/35, br. (1-4), 2002, str. 41-44. https://hrcak.srce.hr/190678. Citirano 28.10.2020.
Chicago 17th Edition
Pušeljić, Silvija, Vesna Milas, Mirna Sipl i Ivo Pušeljić. "Clinical expression of Duchenne and Becker muscular dystrophy with respect to manifestation in the area of Xp21.2 - locus which codifies dystrophin synthesis." Medicinski vjesnik 34/35, br. (1-4) (2002): 41-44. https://hrcak.srce.hr/190678
Harvard
Pušeljić, S., et al. (2002). 'Clinical expression of Duchenne and Becker muscular dystrophy with respect to manifestation in the area of Xp21.2 - locus which codifies dystrophin synthesis', Medicinski vjesnik, 34/35((1-4)), str. 41-44. Preuzeto s: https://hrcak.srce.hr/190678 (Datum pristupa: 28.10.2020.)
Vancouver
Pušeljić S, Milas V, Sipl M, Pušeljić I. Clinical expression of Duchenne and Becker muscular dystrophy with respect to manifestation in the area of Xp21.2 - locus which codifies dystrophin synthesis. Medicinski vjesnik [Internet]. 2002 [pristupljeno 28.10.2020.];34/35((1-4)):41-44. Dostupno na: https://hrcak.srce.hr/190678
IEEE
S. Pušeljić, V. Milas, M. Sipl i I. Pušeljić, "Clinical expression of Duchenne and Becker muscular dystrophy with respect to manifestation in the area of Xp21.2 - locus which codifies dystrophin synthesis", Medicinski vjesnik, vol.34/35, br. (1-4), str. 41-44, 2002. [Online]. Dostupno na: https://hrcak.srce.hr/190678. [Citirano: 28.10.2020.]
Puni tekst: hrvatski, pdf (2 MB) str. 41-44 preuzimanja: 108* citiraj
APA 6th Edition
Pušeljić, S., Milas, V., Sipl, M. i Pušeljić, I. (2002). Klinička ekspresija Duchenneove i Beckerove mišićne distrofije s obzirom na promjene u području Xp21.2 - lokusu koji kodira sintezu distrofina. Medicinski vjesnik, 34/35 ((1-4)), 41-44. Preuzeto s https://hrcak.srce.hr/190678
MLA 8th Edition
Pušeljić, Silvija, et al. "Klinička ekspresija Duchenneove i Beckerove mišićne distrofije s obzirom na promjene u području Xp21.2 - lokusu koji kodira sintezu distrofina." Medicinski vjesnik, vol. 34/35, br. (1-4), 2002, str. 41-44. https://hrcak.srce.hr/190678. Citirano 28.10.2020.
Chicago 17th Edition
Pušeljić, Silvija, Vesna Milas, Mirna Sipl i Ivo Pušeljić. "Klinička ekspresija Duchenneove i Beckerove mišićne distrofije s obzirom na promjene u području Xp21.2 - lokusu koji kodira sintezu distrofina." Medicinski vjesnik 34/35, br. (1-4) (2002): 41-44. https://hrcak.srce.hr/190678
Harvard
Pušeljić, S., et al. (2002). 'Klinička ekspresija Duchenneove i Beckerove mišićne distrofije s obzirom na promjene u području Xp21.2 - lokusu koji kodira sintezu distrofina', Medicinski vjesnik, 34/35((1-4)), str. 41-44. Preuzeto s: https://hrcak.srce.hr/190678 (Datum pristupa: 28.10.2020.)
Vancouver
Pušeljić S, Milas V, Sipl M, Pušeljić I. Klinička ekspresija Duchenneove i Beckerove mišićne distrofije s obzirom na promjene u području Xp21.2 - lokusu koji kodira sintezu distrofina. Medicinski vjesnik [Internet]. 2002 [pristupljeno 28.10.2020.];34/35((1-4)):41-44. Dostupno na: https://hrcak.srce.hr/190678
IEEE
S. Pušeljić, V. Milas, M. Sipl i I. Pušeljić, "Klinička ekspresija Duchenneove i Beckerove mišićne distrofije s obzirom na promjene u području Xp21.2 - lokusu koji kodira sintezu distrofina", Medicinski vjesnik, vol.34/35, br. (1-4), str. 41-44, 2002. [Online]. Dostupno na: https://hrcak.srce.hr/190678. [Citirano: 28.10.2020.]

Sažetak
The role of dystrophin in various clinical presentations of muscular dystrophy is described. Dystrophin is a very complex protein, and the gene coding its synthesis is one of the largest ones in the human genome, occupying about 1 percent of the X-chromosome. Deletions, duplications or point mutations of this huge gene may result in various clinical manifestations ranging from mild muscular fatigue to lethal forms of Duchenne muscular dystrophy.

Ključne riječi
Dystrophin; Duchenne and Becker muscular dystrophy; Area of Xp2l.2-locus

Hrčak ID: 190678

URI
https://hrcak.srce.hr/190678

[hrvatski]

Posjeta: 754 *