Molecular Characterization of a Patient Presumed to Have Prader-Willi Syndrome

Molecular Characterization of a Patient Presumed to Have Prader-Willi Syndrome

Prader-Willi syndrome (PWS) is caused by the loss of RNA expression from an imprinted region on chromosome 15 that includes SNRPN, SNORD115, and SNORD116. Currently, there are no mouse models that faithfully reflect the human phenotype and investigations rely on human post-mortem material. During mo...

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Bibliographic Details
Main Authors: Falaleeva, Marina, Sulsona, Carlos R., Zielke, Horst R., Currey, Kathleen M., de la Grange, Pierre, Aslanzadeh, Vahid, Driscoll, Daniel J., Stamm, Stefan
Format: Online
Language:English
Published: Libertas Academica 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656643/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656643/

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