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Newborn Genetic Screening: Significance in Early Diagnosis of an Infant with Mitochondrial DNA Depletion Syndrome-6

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References

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Acknowledgments

The authors would like to thank Gupte hospital, Pune for providing the medical history of the patients for the study. No research funding was used for this report.

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Authors and Affiliations

  1. Gupte Hospital, Postgraduate Institution and Centre of Research in Reproduction, Pune, Maharashtra, India

    Sanjay A. Gupte & Shweta M. Jangam

  2. Greenarray Genomic Research and Solutions, a division of Accurate Diagnostics Pvt. Ltd., Kothrud, Pune, Maharashtra, India

    Sanjay A. Gupte, Manju Kurup, Preeti Arora & Sarjan S. Shah

Authors
  1. Sanjay A. Gupte
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  2. Manju Kurup
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  3. Shweta M. Jangam
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  4. Preeti Arora
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  5. Sarjan S. Shah
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Corresponding author

Correspondence to Sanjay A. Gupte.

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The authors declare no conflicts of interest.

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We ensure that this work is original and has not been published elsewhere, nor it is currently under consideration for publication elsewhere. We also acknowledge, that all authors have substantially contributed to the underlying research and drafting of this manuscript and agree with the content of the manuscript. We have no conflicts of interest to disclose.

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Sanjay Gupte: Founder, Gynecologist; Manju Kurup: Genetic Counsellor; Shweta Jangam: Clinical Bioinformatician; Preeti Arora: Senior Genomic Scientist; Sarjan Shah: Director.

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Gupte, S.A., Kurup, M., Jangam, S.M. et al. Newborn Genetic Screening: Significance in Early Diagnosis of an Infant with Mitochondrial DNA Depletion Syndrome-6. J Obstet Gynecol India 74, 176–178 (2024). https://doi.org/10.1007/s13224-023-01770-y

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  • DOI: https://doi.org/10.1007/s13224-023-01770-y

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