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Neuropharmacology, ISSN 0028-3908, 12/2013, Volume 75, pp. 549 - 556
Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant disease that results in visible developmental anomalies of the limbs, face, eyes and teeth.... 
Stroke | Hemichannels | Connexin43 | Rare genetic disease | Gap junctional communication | Astrocytes | Pharmacology & Pharmacy | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Foot Deformities, Congenital - genetics | Syndactyly - pathology | Cell Death - genetics | Tooth Abnormalities - complications | Craniofacial Abnormalities - pathology | Foot Deformities, Congenital - complications | Cell Death - drug effects | Neurons - drug effects | Craniofacial Abnormalities - complications | Craniofacial Abnormalities - genetics | Connexin 43 - genetics | Disease Models, Animal | Foot Deformities, Congenital - pathology | Syndactyly - complications | Astrocytes - drug effects | Gap Junctions - pathology | Tooth Abnormalities - genetics | Connexin 43 - metabolism | Glutamic Acid - pharmacology | Mice, Inbred C57BL | Cells, Cultured | Enzyme Inhibitors - pharmacology | Serine - genetics | Mice, Transgenic | Brain Ischemia - physiopathology | Eye Abnormalities - genetics | Mutation - genetics | Brain Infarction - etiology | Animals | Eye Abnormalities - pathology | Tooth Abnormalities - pathology | Connexin 43 - antagonists & inhibitors | Mice | Eye Abnormalities - complications | Syndactyly - genetics | Dysplasia | Gene mutations | Glycine | Glutamate | Analysis | Index Medicus
Journal Article
Rapid communications in mass spectrometry, ISSN 0951-4198, 06/2018, Volume 32, Issue 12, pp. 951 - 958
Journal Article