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Deciphering genetic signatures by whole exome sequencing in a case of co-prevalence of severe renal hypouricemia and diabetes with impaired insulin secretion.

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Title: Deciphering genetic signatures by whole exome sequencing in a case of co-prevalence of severe renal hypouricemia and diabetes with impaired insulin secretion.
Authors: Sekiya, Motohiro1 (AUTHOR), Matsuda, Takaaki1 (AUTHOR), Yamamoto, Yuki1 (AUTHOR), Furuta, Yasuhisa1 (AUTHOR), Ohyama, Mariko1 (AUTHOR), Murayama, Yuki1 (AUTHOR), Sugano, Yoko1 (AUTHOR), Ohsaki, Yoshinori1 (AUTHOR), Iwasaki, Hitoshi1 (AUTHOR), Yahagi, Naoya1 (AUTHOR), Yatoh, Shigeru1 (AUTHOR), Suzuki, Hiroaki1 (AUTHOR), Shimano, Hitoshi1 (AUTHOR) hshimano@md.tsukuba.ac.jp
Source: BMC Medical Genetics. 5/6/2020, Vol. 21 Issue 1, p1-9. 9p.
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genetics%22">BMC Medical Genetics</searchLink>. 5/6/2020, Vol. 21 Issue 1, p1-9. 9p.
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