Found: 6
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Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 8, p. 1, doi. 10.1371/journal.pgen.1007504
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- Publication type:
- Article
Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Cover Image.
- Published in:
- Developmental Neurobiology (19328451), 2016, v. 76, n. 10, p. i, doi. 10.1002/dneu.22432
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- Publication type:
- Article
Drebrin coordinates the actin and microtubule cytoskeleton during the initiation of axon collateral branches.
- Published in:
- Developmental Neurobiology (19328451), 2016, v. 76, n. 10, p. 1092, doi. 10.1002/dneu.22377
- By:
- Publication type:
- Article
Views of newly-qualified GPs about their training and preparedness: lessons for extended generalist training.
- Published in:
- British Journal of General Practice, 2015, v. 65, n. 633, p. e270, doi. 10.3399/bjgp15X684445
- By:
- Publication type:
- Article
Probiotics, Prebiotics and Immunomodulation of Gut Mucosal Defences: Homeostasis and Immunopathology.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article