“DEL16P12.1P11.2”的意思、由来-开放百科全书

词条

DEL16P12.1P11.2

释义

References

Chromosome 16p12.2-p11.2 deletion syndrome is a protein that in humans is encoded by the DEL16P12.1P11.2 gene.

^[1]

References

1. ^{{cite web| title = Entrez Gene: Chromosome 16p12.2-p11.2 deletion syndrome| url = https://www.ncbi.nlm.nih.gov/gene/100526742| accessdate = 2014-03-12 }}

2 : Genes|Human proteins

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