Patients’ Opinions on Genetic Counseling on the Increased Risk of Parkinson Disease among Gaucher Disease Carriers
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/article/10.1007/s10897-017-0161-0/fulltext.html
Reference14 articles.
1. ACOG Committee on Genetics. (2009). ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of Eastern European Jewish descent. Obstetrics and Gynecology, 114(4), 950–953. https://doi.org/10.1097/AOG.0b013e3181bd12f4 .
2. Alcalay, R. N., Dinur, T., Quinn, T., Sakanaka, K., Levy, O., Waters, C., et al. (2014). Comparison of Parkinson risk in Ashkenazi Jewish patients with Gaucher disease and GBA heterozygotes. JAMA Neurology, 71(6), 752–757. https://doi.org/10.1001/jamaneurol.2014.313 .
3. Anheim, M., Elbaz, A., Lesage, S., Durr, A., Condroyer, C., Viallet, F., et al. (2012). Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers. Neurology, 78(6), 417–420. https://doi.org/10.1212/WNL.0b013e318245f476 .
4. Balwani, M., Fuerstman, L., Kornreich, R., Edelmann, L., & Desnick, R. J. (2010). Type 1 Gaucher disease: significant disease manifestations in "asymptomatic" homozygotes. Archives of Internal Medicine, 170(16), 1463–1469. https://doi.org/10.1001/archinternmed.2010.302 .
5. Beavan, M. S., & Schapira, A. H. (2013). Glucocerebrosidase mutations and the pathogenesis of Parkinson disease. Annals of Medicine, 45(8), 511–521. https://doi.org/10.3109/07853890.2013.849003 .
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