Journals / Turkish Journal of Medical Sciences / 2005 / Cilt: 35 - Sayı: 3

Wolfram Syndrome (WS), Neither an Autosomal Nor a Sex Linked Disorder

Pages
193–193
Publication Date
2022-11-05
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Full text: pdf Other articles published in the same issue: Turk J Med Sci,vol.35,iss.3.

📌 3 Key Takeaways

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Objective & Hypothesis:Turk J Med Sci 2005; 35(3): 193.
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Key Findings & Data:Turk J Med Sci 2005; 35(3): 193.
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Conclusion & Impact:Full text: pdf Other articles published in the same issue: Turk J Med Sci,vol.35,iss.3.
🔬Design:Research Article
📍Scope:2005 Verileri
⚙️Variables:Domain Parameters

Abstract

Turk J Med Sci 2005; 35(3): 193. Full text: pdf Other articles published in the same issue: Turk J Med Sci,vol.35,iss.3.

Özet

Turk J Med Sci 2005; 35(3): 193. Full text: pdf Other articles published in the same issue: Turk J Med Sci,vol.35,iss.3.

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Cite This Article

ÖZSOYLU, Ş. (2022). Wolfram Syndrome (WS), Neither an Autosomal Nor a Sex Linked Disorder. Turkish Journal of Medical Sciences, Cilt: 35 - Sayı: 3, 193–193. https://ajindex.com/articles/612001

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References (3)

  1. Kabakufl N, Çıtak-Kurt AN, Kurt A et al. Additional distinct findings in three cases with Wolfram syndrome Turk J Med Sci: 51-55, 2005.
  2. Schwartz M, Vissing J. Paternal inheritance of mitochondrial DNA. N Engl J Med 347: 576-578, 2002.
  3. Chinnery PE, Di Mauro S, Shanske S et al. Risk of developing a mitochondrial DNA deletion disorder. Lancet 364: 592-596,