Monaco A P
Wellcome Trust Centre for Human Genetics, University of Oxford, UK.
Curr Biol. 1996 Nov 1;6(11):1396-8. doi: 10.1016/s0960-9822(96)00740-3.
Molecular analysis of a small hemizygous deletion in a patient with partial Williams syndrome suggests that loss of the LIM-Kinase1 gene may be responsible for the impaired visuospatial constructive cognition characteristic of the syndrome.
对一名部分威廉姆斯综合征患者的小的半合子缺失进行分子分析表明，LIM激酶1基因的缺失可能是该综合征特征性的视觉空间建构认知受损的原因。
