Molecular diagnosis of Kallmann syndrome with diabetes by whole exome sequencing and bioinformatic approaches

doi:10.4239/wjd.v12.i12.2058

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Dec 15, 2021 (publication date) through Jun 28, 2024

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World Journal of Diabetes

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1948-9358

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Diabetes. Dec 15, 2021; 12(12): 2058-2072
Published online Dec 15, 2021. doi: 10.4239/wjd.v12.i12.2058

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Figure 1 Intersection analysis of Kallmann syndrome and normosmic hypogonadotropic hypogonadism pathogenic genes. nIHH: Normosmic hypogonadotropic hypogonadism; KS: Kallmann syndrome.

Citation: Sun SS, Wang RX. Molecular diagnosis of Kallmann syndrome with diabetes by whole exome sequencing and bioinformatic approaches. World J Diabetes 2021; 12(12): 2058-2072
URL: https://www.wjgnet.com/1948-9358/full/v12/i12/2058.htm
DOI: https://dx.doi.org/10.4239/wjd.v12.i12.2058