Tag Prader-Willi Syndrome

Prader-Willi Syndrome

Prader-Will Syndrome is caused by genetic variation. A rare genetic condition, due to deletion of chromosome 15, is located at chr15q11.2. Imprinted genes of NPAP1/C15orf2. NAPAP1 stands for Nuclear Pore Associated Protein 1. Due to a heterozygous deletion of chromosome… Continue Reading →

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