chromosomal translocation t(16;22)(p13.3;q11.2)

From Aaushi

Jump to navigation Jump to search

^[1]

Introduction

chromosomal translocation t(16;22)(p13.3;q11.2) involving TMEM114 may be a cause of congenital & juvenile cataracts

More general terms

chromosomal translocation

References

↑ UniProt http://www.uniprot.org/uniprot/B3SHH9.html

Retrieved from "https://aaushi.info/w/index.php?title=A25087&oldid=963570"

↑ Back to top