ss20399075

A SNP located within the 3' UTR of FGF20, is significantly associated with PD risk

Identifier

CONSO00139

Type

genetic variant

Author

Lingling Xu

https://orcid.org/0000-0002-0303-8616

References

• pubmed:15122513

Cross-references

None available.

Synonyms

None available.

Incoming Relations

None available.

Outgoing Relations

None available.