| Case Report Online Published: 06 Dec 2018 | ||||||||||||
A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia Amrit Bhangoo, Peter Zhan Tao Wang, Irene Young, Aaron Sassoon, Roberto Taguibao, Antoine Khoury.
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| How to Cite this Article |
| Pubmed Style Bhangoo A, Wang PZT, Young I, Sassoon A, Taguibao R, Khoury A. A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia. Int J Med Rev Case Rep. 2019; 3(2): 87-90. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation Web Style Bhangoo A, Wang PZT, Young I, Sassoon A, Taguibao R, Khoury A. A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia. https://www.mdpub.net/?mno=5455 [Access: October 13, 2024]. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation AMA (American Medical Association) Style Bhangoo A, Wang PZT, Young I, Sassoon A, Taguibao R, Khoury A. A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia. Int J Med Rev Case Rep. 2019; 3(2): 87-90. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation Vancouver/ICMJE Style Bhangoo A, Wang PZT, Young I, Sassoon A, Taguibao R, Khoury A. A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia. Int J Med Rev Case Rep. (2019), [cited October 13, 2024]; 3(2): 87-90. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation Harvard Style Bhangoo, A., Wang, . P. Z. T., Young, . I., Sassoon, . A., Taguibao, . R. & Khoury, . A. (2019) A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia. Int J Med Rev Case Rep, 3 (2), 87-90. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation Turabian Style Bhangoo, Amrit, Peter Zhan Tao Wang, Irene Young, Aaron Sassoon, Roberto Taguibao, and Antoine Khoury. 2019. A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia. International Journal of Medical Reviews and Case Reports, 3 (2), 87-90. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation Chicago Style Bhangoo, Amrit, Peter Zhan Tao Wang, Irene Young, Aaron Sassoon, Roberto Taguibao, and Antoine Khoury. "A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia." International Journal of Medical Reviews and Case Reports 3 (2019), 87-90. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation MLA (The Modern Language Association) Style Bhangoo, Amrit, Peter Zhan Tao Wang, Irene Young, Aaron Sassoon, Roberto Taguibao, and Antoine Khoury. "A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia." International Journal of Medical Reviews and Case Reports 3.2 (2019), 87-90. Print. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation APA (American Psychological Association) Style Bhangoo, A., Wang, . P. Z. T., Young, . I., Sassoon, . A., Taguibao, . R. & Khoury, . A. (2019) A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia. International Journal of Medical Reviews and Case Reports, 3 (2), 87-90. doi:10.5455/IJMRCR.Leydig-cell-hyperplasia-mutation |
