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Hypertrophic Cardiomyopathy with Familial Chylomicronemia Syndrome: Is it an Incidental Finding or a New Association?

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References

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Contributions

MG, EÖ and FE: Drafted the manuscript. All authors participated in the follow-up and management of the patient and approved the final version. MG will act as guarantor for this paper.

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Authors and Affiliations

  1. Division of Nutrition and Metabolism, The Ministry of Health, Ankara Children’s Health and Diseases Hematology- Oncology Training and Research Hospital, Ankara, Turkey

    Mehmet Gündüz & Nevra Koç

  2. Infancy Service, The Ministry of Health, Ankara Children’s Health and Diseases Hematology- Oncology Training and Research Hospital, Ankara, Turkey

    Eda Özaydın

  3. Department of Pediatric Cardiology, Ankara Children’s Health and Diseases Hematology- Oncology Training and Research Hospital, Ankara, Turkey

    Filiz Ekici

Authors
  1. Mehmet Gündüz
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  2. Nevra Koç
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  3. Eda Özaydın
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  4. Filiz Ekici
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Corresponding author

Correspondence to Eda Özaydın.

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Gündüz, M., Koç, N., Özaydın, E. et al. Hypertrophic Cardiomyopathy with Familial Chylomicronemia Syndrome: Is it an Incidental Finding or a New Association?. Indian J Pediatr 81, 1111–1112 (2014). https://doi.org/10.1007/s12098-013-1331-1

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  • DOI: https://doi.org/10.1007/s12098-013-1331-1

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