Pub. Date : 2006 Nov
PMID : 17024248
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Smith-Magenis syndrome is associated with a 3.7-Mb deletion in 17p11.2, and its clinical presentation is caused by retinoic acid inducible 1 (RAI1) haploinsufficiency. | Tretinoin | retinoic acid induced 1 | Mus musculus |