Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophies
Patel, N., Alkuraya, H., Alzahrani, S.S., Nowailaty, S.R., Seidahmed, M.Z., Alhemidan, A., Ben‐Omran, T., Ghazi, N.G., Al‐Aqeel, A., Al‐Owain, M., Alzaidan, H.I., Faqeih, E., Kurdi, W., Rahbeeni, Z., Ibrahim, N., Abdulwahab, F., Hashem, M., Shaheen, R., Abouelhoda, M., Monies, D., Khan, A.O., Aldahmesh, M.A., Alkuraya, Fowzan S.
Published in Clinical genetics (01.12.2018)
Published in Clinical genetics (01.12.2018)
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