Localization of the Norrie disease gene mRNA by in situ hybridization

Norrie disease is a rare X-linked recessive neurodevelopmental disorder. The affected males manifest congenital blindness, which is often associated with hearing loss, mental retardation and psychiatric problems. Genetic linkage studies have localized the gene to the short arm of the X-chromosome an...

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Bibliographic Details
Published in:	Brain research bulletin Vol. 49; no. 5; pp. 355 - 358
Main Authors:	Hartzer, Michael K, Cheng, Mei, Liu, X, Shastry, Barkur S
Format:	Journal Article
Language:	English
Published:	New York, NY Elsevier Inc 15-07-1999 Elsevier Science
Subjects:	Animals Biological and medical sciences Brain - metabolism Cerebellum Eye Proteins - genetics Ganglion cells Hippocampus Humans In Situ Hybridization Malformations of the eye Medical sciences Mice mRNA Nerve Tissue Proteins - genetics Ophthalmology Rabbits Retina - metabolism RNA, Messenger - metabolism Tissue Distribution - physiology Cerebellum mRNA Ganglion cells Hippocampus Human Molecular hybridization Nervous system diseases Norrie disease Retinopathy Rodentia Central nervous system Rabbit Lagomorpha Genetic disease Ganglion neuron Eye disease Vertebrata Mammalia Messenger RNA Gene Mouse ENT disease Localization Brain (vertebrata)
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