Tricellulin Is a Tight-Junction Protein Necessary for Hearing
Riazuddin, Saima, Ahmed, Zubair M., Fanning, Alan S., Lagziel, Ayala, Kitajiri, Shin-ichiro, Ramzan, Khushnooda, Khan, Shaheen N., Chattaraj, Parna, Friedman, Penelope L., Anderson, James M., Belyantseva, Inna A., Forge, Andrew, Riazuddin, Sheikh, Friedman, Thomas B.
Published in American journal of human genetics (01.12.2006)
Published in American journal of human genetics (01.12.2006)
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Journal Article
Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86
Rehman, Atteeq U., Santos-Cortez, Regie Lyn P., Morell, Robert J., Drummond, Meghan C., Ito, Taku, Lee, Kwanghyuk, Khan, Asma A., Basra, Muhammad Asim R., Wasif, Naveed, Ayub, Muhammad, Ali, Rana A., Raza, Syed I., Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael, Riazuddin, Saima, Billington, Neil, Khan, Shaheen N., Friedman, Penelope L., Griffith, Andrew J., Ahmad, Wasim, Riazuddin, Sheikh, Leal, Suzanne M., Friedman, Thomas B.
Published in American journal of human genetics (02.01.2014)
Published in American journal of human genetics (02.01.2014)
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Journal Article
Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome
Riazuddin, Saima, Anwar, Saima, Fischer, Martin, Ahmed, Zubair M., Khan, Shahid Y., Janssen, Audrey G.H., Zafar, Ahmad U., Scholl, Ute, Husnain, Tayyab, Belyantseva, Inna A., Friedman, Penelope L., Riazuddin, Sheikh, Friedman, Thomas B., Fahlke, Christoph
Published in American journal of human genetics (14.08.2009)
Published in American journal of human genetics (14.08.2009)
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Journal Article
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss
Nayak, Gowri, Varga, Lukas, Trincot, Claire, Shahzad, Mohsin, Friedman, Penelope L., Klimes, Iwar, Greinwald, John H., Riazuddin, S. Amer, Masindova, Ivica, Profant, Milan, Khan, Shaheen N., Friedman, Thomas B., Ahmed, Zubair M., Gasperikova, Daniela, Riazuddin, Sheikh, Riazuddin, Saima
Published in Human genetics (01.04.2015)
Published in Human genetics (01.04.2015)
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Journal Article
Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness
Riazuddin, Saima, Khan, Shaheen N., Ahmed, Zubair M., Ghosh, Manju, Caution, Kyle, Nazli, Sabiha, Kabra, Madhulika, Zafar, Ahmad U., Chen, Kevin, Naz, Sadaf, Antonellis, Anthony, Pavan, William J., Green, Eric D., Wilcox, Edward R., Friedman, Penelope L., Morell, Robert J., Riazuddin, Sheikh, Friedman, Thomas B.
Published in American journal of human genetics (01.01.2006)
Published in American journal of human genetics (01.01.2006)
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Journal Article
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome
Faridi, R., Rehman, A.U., Morell, R.J., Friedman, P.L., Demain, L., Zahra, S., Khan, A.A., Tohlob, D., Assir, M.Z., Beaman, G., Khan, S.N., Newman, W.G., Riazuddin, S., Friedman, T.B.
Published in Clinical genetics (01.02.2017)
Published in Clinical genetics (01.02.2017)
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Journal Article
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23
Ahmed, ZM, Riazuddin, S, Khan, SN, Friedman, PL, Riazuddin, S, Friedman, TB
Published in Clinical genetics (01.01.2009)
Published in Clinical genetics (01.01.2009)
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