Found: 5
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Kleefstra-variant syndrome with heterozygous mutations in EHMT1 and KCNQ2 genes: a case report.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
An Overview of Candidate Therapeutic Target Genes in Ovarian Cancer.
- Published in:
- Cancers, 2020, v. 12, n. 6, p. 1470, doi. 10.3390/cancers12061470
- By:
- Publication type:
- Article
Identification of a novel truncating mutation in PALB2 gene by a multigene sequencing panel for mutational screening of breast cancer risk-associated and related genes.
- Published in:
- 2018
- By:
- Publication type:
- journal article
The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from Southern Italy.
- Published in:
- Movement Disorders, 2011, v. 26, n. 9, p. 1732, doi. 10.1002/mds.23735
- By:
- Publication type:
- Article
Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit.
- Published in:
- Movement Disorders, 2011, v. 26, n. 4, p. 739, doi. 10.1002/mds.23435
- By:
- Publication type:
- Article