Colocalization of Oxtr with Prader-Willi Syndrome transcripts in the trigeminal ganglion of neonatal mice - Archive ouverte HAL Access content directly
Journal Articles Human Molecular Genetics Year : 2020

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hal-02635677 , version 1 (27-05-2020)

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Radhika Vaidyanathan, Fabienne Schaller, Françoise Muscatelli, Elizabeth Hammock. Colocalization of Oxtr with Prader-Willi Syndrome transcripts in the trigeminal ganglion of neonatal mice. Human Molecular Genetics, 2020, ⟨10.1093/hmg/ddaa094⟩. ⟨hal-02635677⟩
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