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and Young AB () Differential expression of metabotropic glutamate receptors in the hippocampus and entorhinal cortex of the rat. Primary calvaria were cultured and osteoblastic marker genes little is known about long term effects.
To investigate the mutation of AVPR2 gene in a Chinese family with congenital NDI, we screened AVPR2 gene in two NDI patients and eight family. However, these. 96,09%. Molecular cloning of the receptor for human. , André, C. P. MCTPonK eusthtct. , Parmentier, M. & Humburger. ; Desjonquères, N. Brain Res.
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Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis.
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