INHERITANCE IN MITOCHONDRIAL GENOME AND ITS RELATED DISEASES

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MOROVVATI SAEID

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

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Journal: Journal of Medical Council of Iran Year:2010 | Volume:28 | Issue:3 Page(s): 314-325

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Information Journal Paper

Title

INHERITANCE IN MITOCHONDRIAL GENOME AND ITS RELATED DISEASES

Author(s)

MOROVVATI SAEID | Issue Writer Certificate

Keywords

MTDNAQ3

MITOCHONDRIAL DISEASESQ3

MATERNAL INHERITANCEQ3

Abstract

Mitochondria are ubiquitous in eukaryotes and are essential for survival. Their primary function is to support aerobic respiration and to provide energy substrates for intracellular metabolic pathways. Given its fundamental role in the human body, defects of mitochondrial function can have disastrous consequences.Human MITOCHONDRIAL DISEASES encompass mutations of MTDNA and nuclear DNA. This review aims to provide an update on the involvement of mitochondrial DNA in human disease, its inheritance pattern and relationship between genotype and phenotype in MITOCHONDRIAL DISEASES. Improved understanding of MTDNA inheritance and mutation penetrance patterns, offer significant prospects for more accurate genetic counselling and effective future therapies.

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APA: Copy

MOROVVATI, SAEID. (2010). INHERITANCE IN MITOCHONDRIAL GENOME AND ITS RELATED DISEASES. JOURNAL OF MEDICAL COUNCIL OF I.R.I., 28(3), 314-325. SID. https://sid.ir/paper/41319/en

Vancouver: Copy

MOROVVATI SAEID. INHERITANCE IN MITOCHONDRIAL GENOME AND ITS RELATED DISEASES. JOURNAL OF MEDICAL COUNCIL OF I.R.I.[Internet]. 2010;28(3):314-325. Available from: https://sid.ir/paper/41319/en

IEEE: Copy

SAEID MOROVVATI, “INHERITANCE IN MITOCHONDRIAL GENOME AND ITS RELATED DISEASES,” JOURNAL OF MEDICAL COUNCIL OF I.R.I., vol. 28, no. 3, pp. 314–325, 2010, [Online]. Available: https://sid.ir/paper/41319/en

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