A disease specific questionnaire for assessing behavior in individuals with Prader-Willi syndrome
A disease specific questionnaire for assessing behavior in individuals with Prader-Willi syndrome
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DOI：
10.1016/j.comppsych.2014.12.005
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发表时间：
2015-04-01
影响因子：
7.3
通讯作者：
Benarroch, Fortu
中科院分区：
文献类型：
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作者：
Avrahamy, Hamutal;Pollak, Yehuda;Benarroch, Fortu
目的：Prader-Willi综合征（PWS）是一种遗传性多系统疾病，伴有多种医学、认知、行为和精神问题。PWS是由于染色体15 q2-q13上的父本基因缺失（70-75%）、单亲二体性（25-30%）或印记中心缺陷（
Objective: Prader Willi syndrome (PWS) is a genetic multisystem disorder with various medical, cognitive, behavioral and psychiatric problems. PWS is caused by the lack of expression of paternal genes on chromosome 15q2-q13 due to a deletion (70-75%), uniparental disomy (25-30%) or imprinting center defect (