المؤلفون: Peng, Yanyan, Shinde, Deepali N, Valencia, C Alexander, Mo, Jun-Song, Rosenfeld, Jill, Cho, Megan Truitt, Chamberlin, Adam, Li, Zhuo, Liu, Jie, Gui, Baoheng, Brockhage, Rachel, Basinger, Alice, Alvarez-Leon, Brenda, Heydemann, Peter, Magoulas, Pilar L, Lewis, Andrea M, Scaglia, Fernando, Gril, Solange, Chong, Shuk Ching, Bower, Matthew, Monaghan, Kristin G, Willaert, Rebecca, Plona, Maria-Renee, Dineen, Rich, Milan, Francisca, Hoganson, George, Powis, Zoe, Helbig, Katherine L, Keller-Ramey, Jennifer, Harris, Belinda, Anderson, Laura C, Green, Torrian, Rizzo, Stacey J Sukoff, Kaylor, Julie, Chen, Jiani, Guan, Min-Xin, Sellars, Elizabeth, Sparagana, Steven P, Gibson, James B, Reinholdt, Laura G, Tang, Sha, Huang, Taosheng

المصدر: Human Molecular Genetics. 26(24)

مصطلحات موضوعية: Neurosciences, Eye Disease and Disorders of Vision, Genetics, Clinical Research, Aetiology, 2.1 Biological and endogenous factors, Neurological, Adolescent, Alleles, Animals, Child, Child, Preschool, Electron Transport, Female, Ferredoxins, Humans, Infant, Iron, Iron-Sulfur Proteins, Male, Mice, Mitochondria, Mitochondrial Membranes, Mutagenesis, Mutation, Optic Atrophy, Oxidoreductases, Pedigree, Sulfite Reductase (Ferredoxin), Exome Sequencing, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/1pd479ht

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المؤلفون: Yanyan Peng, Shinde, Deepali N., Valencia, C. Alexander, Jun-Song Mo, Rosenfeld, Jill, Cho, Megan Truitt, Chamberlin, Adam, Zhuo Li, Jie Liu, Baoheng Gui, Brockhage, Rachel, Basinger, Alice, Alvarez-Leon, Brenda, Heydemann, Peter, Magoulas, Pilar L., Lewis, Andrea M., Scaglia, Fernando, Gril, Solange, Shuk Ching Chong, Bower, Matthew

المصدر: Human Molecular Genetics; 12/15/2017, Vol. 26 Issue 24, p4937-4950, 14p

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