Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

标题
Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume -, Issue -, Pages -
出版商
Oxford University Press (OUP)
发表日期
2018-09-19
DOI
10.1093/hmg/ddy337

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