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Whole Exome Sequencing Identifies Mutations in GNB3 to Cause a Novel Congenital Stationary Night Blindness Phenotype
Whole Exome Sequencing Identifies Mutations in GNB3 to Cause a Novel Congenital Stationary Night Blindness Phenotype
2016
Ajoy Vincent
Erika S. Tavares
Isabelle Audo
Jason T. Maynes
Shuning Li
Christelle Michiels
Anupreet Tumber
Heather MacDonald
Chelsea Roadhouse
Christina Zeitz
Elise Héon
Keywords:
Exome sequencing
GNB3
Congenital stationary night blindness
Phenotype
Genetics
Biology
Correction
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