相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。LOXL3, encoding lysyl oxidase-like 3, is mutated in a family with autosomal recessive Stickler syndrome
Fatema Alzahrani et al.
HUMAN GENETICS (2015)
Loss of lysyl oxidase-like 3 causes cleft palate and spinal deformity in mice
Jian Zhang et al.
HUMAN MOLECULAR GENETICS (2015)
A tissue-specific variant of the human lysyl oxidase-like protein 3 (LOXL3) functions as an amine oxidase with substrate specificity
Jae-Eun Lee et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Lysyl oxidase: an oxidative enzyme and effector of cell function
H. A. Lucero et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2006)
Stickler syndrome: Clinical characteristics and diagnostic criteria
PS Rose et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)