IMD33 |
IMD38 |
60S ribosomal protein L31 |
||
[immunodeficiency 37] this is a databank designation of an immunodeficiency disorder caused by homozygous mutations in the gene encoding BCL10 (see).
For other entries pertaining to hematopoiesis see also the Hematology Dictionary section of this encyclopedia.
... ... ... ...| SUPPORT COPE | Intro | Subdictionaries | New Entries | Contribute data | COPE Credentials |
| # | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z |
|
Created, developed, and maintained by Dr H Ibelgaufts
|
U L T R A P O S S E N E M O O B L I G A T U R