Ullrich Konjenital Muskuler Distrofinin Prenatal Tanısı
Abstract
Keywords
References
- Karpati G, Hilton-Jones D, Griggs RC. Disorders of voluntary muscle: Cambridge University Press; 2001.
- Haliloglu G, Topaloglu H. Ullrich Congenital Muscular Dystrophy. Iranian Journal of Child Neurology. 2011;5(3):1-13.
- Timpl R, Chu M-L. Microfibrillar collagen type VI. Extracellular matrix as- sembly and structure. 1994:208-42.
- Weil D, Mattei M, Passage E, N'Guyen V, Pribula-Conway D, Mann K, et al. Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen. American journal of human genetics. 1988;42(3):435.
- Kuo H-J, Maslen CL, Keene DR, Glanville RW. Type VI collagen anchors endothelial basement membranes by interacting with type IV collagen. Journal of Biological Chemistry. 1997;272(42):26522-9.
- Bethlem J, Wijngaarden GK. Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees. Brain: a journal of neurology. 1976;99(1):91-100.
- Paillette L, Aicardi J, Goutières F. Ullrich's congenital atonic sclerotic mus- cular dystrophy. Journal of Neurology. 1989;236(2):108-10.
- Vanegas OC, Bertini E, Zhang R-Z, Petrini S, Minosse C, Sabatelli P, et al. Ullrich scleroatonic muscular dystrophy is caused by recessive mutati- ons in collagen type VI. Proceedings of the National Academy of Scien- ces. 2001;98(13):7516-21.
Details
Primary Language
Turkish
Subjects
-
Journal Section
-
Authors
Canan Ünal
This is me
Erdem Fadıloğlu
This is me
Gonca Özten
This is me
Beril Talim
This is me
Mehmet Sinan Beksaç
This is me
Publication Date
October 1, 2018
Submission Date
-
Acceptance Date
-
Published in Issue
Year 2018 Volume: 15 Number: 4