Deciphering genetic signatures by whole exome sequencing in a case of co-prevalence of severe renal hypouricemia and diabetes with impaired insulin secretion.
Saved in:
| 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. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
Be the first to leave a comment!
