Associated Papers
Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathology.
Enikanolaiye A et al.
Genome Research, 2020
32317254 (PubMed )
Supplement: supp_gr.258400.119_Supplemental_Table_S1_.xlsx › S_165N
[A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13].
Yu ZQ et al.
[zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology, 2007
Familial high myopia: evidence of an autosomal dominant mode of inheritance and genetic heterogeneity.
Naiglin L et al.
Annales De Genetique, 1999
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