In vivo structural neuroimaging evaluation of the hypothalamus in Prader-Willi Syndrome sub-genotypes
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Abstract Purpose Prader-Willi Syndrome (PWS) is a rare genetic disorder with a heterogeneous phenotype, caused by loss of expression of genes on the paternally inherited chromosome 15q11.2-15q13.3, primarily due to pater...
LCC LCC:Specialties of internal medicineIdioma eng
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