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Combined use of genetic and immunohistochemical analysis is a critical step in differential diagnosis of sarcoglycanopathies [J Behcet Uz Child Hosp]
J Behcet Uz Child Hosp. 2017; 7(3): 247-250 | DOI: 10.5222/buchd.2017.247  

Combined use of genetic and immunohistochemical analysis is a critical step in differential diagnosis of sarcoglycanopathies

Gülden Diniz1, Aycan Unalp2, Filiz Hazan2, Figen Özgönül1, Sabiha Türe3, Galip Akhan3
1Tepecik Education And Research Hospital, Pathology And Pediatric Neurology
2Izmir Dr. Behcet Uz Children
3Izmir Katip Celebi University Neurology

Keywords: muscular dystrophy, sarcoglycanopthy, muscle biopsy, genetic test


Genetik ve immünohistokimyasal incelemelerin birlikte kullanımı sarkoglikanopatilerin ayırıcı tanısında önemli bir basamaktır

Gülden Diniz1, Aycan Unalp2, Filiz Hazan2, Figen Özgönül1, Sabiha Türe3, Galip Akhan3
1Tepecik Eğitim Ve Araştırma Hastanesi, Patoloji Ve Pediatrik Nöroloji
2İzmir Dr. Behçet Uz Çocuk Hastalıkları Ve Cerrahisi Eğitim Ve Araştırma Hastanesi, Pediatrik Nöroloji Ve Genetik.
3Izmir Katip Çelebi Üniversitesi, Nöroloji

Anahtar Kelimeler: muskuler distrofi, sarkoglikanopati, kas biyopsisi, genetik test


Gülden Diniz, Aycan Unalp, Filiz Hazan, Figen Özgönül, Sabiha Türe, Galip Akhan. Combined use of genetic and immunohistochemical analysis is a critical step in differential diagnosis of sarcoglycanopathies. J Behcet Uz Child Hosp. 2017; 7(3): 247-250

Corresponding Author: Gülden Diniz, Türkiye


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