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American Journal of Medical Genetics Part A, ISSN 1552-4825, 07/2017, Volume 173, Issue 7, pp. 1951 - 1954
Developmental encephalopathies constitute a broad and genetically heterogeneous spectrum of disorders associated with global developmental delay, intellectual... 
epilepsy | developmental encephalopathy | PLXNA1 | AUTISM | DE-NOVO MUTATIONS | DUBOWITZ-SYNDROME | GENETICS & HEREDITY | IMPLICATE | Epilepsy | Literature reviews | Intellectual disabilities | Encephalopathy
Journal Article
Cell Reports, ISSN 2211-1247, 10/2019, Volume 29, Issue 2, pp. 347 - 362.e5
Accurate perception of guidance cues is crucial for cell and axon migration. During initial navigation in the spinal cord, commissural axons are kept... 
Robo1 | growth cone | Nrp2 | midline | axon guidance | guidance receptors | PlxnA1 | MIDLINE SWITCH | ROLES | IN-VIVO | DYNAMICS | GUIDANCE | PROTEINS | ROBO1 | CELL BIOLOGY | Life Sciences | Development Biology | Cellular Biology | Neurons and Cognition | Neurobiology
Journal Article
Clinical Genetics, ISSN 0009-9163, 02/2019, Volume 95, Issue 2, pp. 320 - 324
Idiopathic hypogonadotropic hypogonadism (IHH) can be divided into two major forms, normosmic IHH and Kallmann syndrome (KS). Genetic mutations are responsible... 
PLXNA1 | oligogenic inheritance | idiopathic hypogonadotropic hypogonadism | Kallmann syndrome | MIGRATION | GENETICS | GENETICS & HEREDITY | DIGENIC MUTATIONS | OLFACTORY SYSTEM | CHALLENGES | Phenotypes | Leukocyte migration | Hedgehog protein | Etiology | Olfaction | Anosmia | Gonadotropin-releasing hormone | Fibroblast growth factor receptor 1 | Hypogonadism | Cell migration
Journal Article
Journal Article
Cytogenetics and Cell Genetics, ISSN 0301-0171, 01/2001, Volume 92, Issue 1-2, pp. 127 - 129
We determined chromosome locations of four plexin A subfamily genes, Plxna1, Plxna2, Plxna3 and Plxna4, in four rodent species, mouse, rat, Syrian hamster and... 
chromosome 4 | chromosome 5 | chromosome 6 | Plxna4 gene | Plxna1 gene | chromosome 1 | Plxna2 gene | chromosome 11 | chromosome 13 | chromosome 8 | Plxna3 gene | plexin A
Journal Article
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