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Autor:
Julian Esteve-Rudd, Stef J.F. Letteboer, Graeme Mardon, Yalda Moayedi, Huidan Xu, Thanh Minh T. Nguyen, Yumei Li, Aiden Eblimit, David L. Simons, Ronald Roepman, Ka Man Wu, Samuel M. Wu, Rui Chen, David S. Williams, Lin Gan, Sylvia E. C. van Beersum, Yiyun Chen, Qian Ding, Hua Zhong, Patrick Pickard, Jeroen van Reeuwijk, Keqing Wang
Publikováno v:
Human Molecular Genetics, 24, 6, pp. 1584-601
Human molecular genetics, vol 24, iss 6
Human Molecular Genetics, 24, 1584-601
Human molecular genetics, vol 24, iss 6
Human Molecular Genetics, 24, 1584-601
Item does not contain fulltext Leber congenital amaurosis (LCA) and juvenile retinitis pigmentosa (RP) are severe hereditary diseases that causes visual impairment in infants and children. SPATA7 has recently been identified as the LCA3 and juvenile