Pub. Date : 2004 Aug
PMID : 15334500
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Variant chronic infantile neurologic, cutaneous, articular syndrome due to a mutation within the leucine-rich repeat domain of CIAS1. | Leucine | NLR family pyrin domain containing 3 | Homo sapiens |