Found: 7
Select item for more details and to access through your institution.
METTL23, a transcriptional partner of GABPA, is essential for human cognition.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 13, p. 3456, doi. 10.1093/hmg/ddu054
- By:
- Publication type:
- Article
A PIECE OF MY MIND. A Wild Rotation.
- Published in:
- 2016
- By:
- Publication type:
- journal article
A Wild Rotation.
- Published in:
- JAMA: Journal of the American Medical Association, 2016, v. 316, n. 7, p. 713, doi. 10.1001/jama.2016.4994
- By:
- Publication type:
- Article
Resolving rates of mutation in the brain using single-neuron genomics.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.12966
- By:
- Publication type:
- Article
Serial enrichment of heteroduplex DNA using a MutS‐magnetic bead system.
- Published in:
- Biotechnology Journal, 2023, v. 18, n. 1, p. 1, doi. 10.1002/biot.202200323
- By:
- Publication type:
- Article
Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 9, p. 1552, doi. 10.1093/hmg/ddac309
- By:
- Publication type:
- Article
Transcriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosis.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1405
- By:
- Publication type:
- Article