Fu, J., Ma, L., Cheng, J., Yang, L., Wei, C., Fu, S., . . . Fu, J. (2018). A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS‐based genetic diagnosis. J Cell Mol Med.
Citação norma ChicagoFu, Jiewen, Lu Ma, Jingliang Cheng, Lisha Yang, Chunli Wei, Shangyi Fu, Hongbin Lv, Rui Chen, and Junjiang Fu. "A Novel, Homozygous Nonsense Variant of the CDHR1 Gene in a Chinese Family Causes Autosomal Recessive Retinal Dystrophy By NGS‐based Genetic Diagnosis." J Cell Mol Med 2018.
Citação norma MLAFu, Jiewen, et al. "A Novel, Homozygous Nonsense Variant of the CDHR1 Gene in a Chinese Family Causes Autosomal Recessive Retinal Dystrophy By NGS‐based Genetic Diagnosis." J Cell Mol Med 2018.