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A mutation in PDS causes non-syndromic recessive deafness.
Li XC, Everett LA, Lalwani AK, Desmukh D, Friedman TB, Green ED, Wilcox ER. Li XC, et al. Among authors: desmukh d. Nat Genet. 1998 Mar;18(3):215-7. doi: 10.1038/ng0398-215. Nat Genet. 1998. PMID: 9500541 No abstract available.
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
Bork JM, Peters LM, Riazuddin S, Bernstein SL, Ahmed ZM, Ness SL, Polomeno R, Ramesh A, Schloss M, Srisailpathy CR, Wayne S, Bellman S, Desmukh D, Ahmed Z, Khan SN, Kaloustian VM, Li XC, Lalwani A, Riazuddin S, Bitner-Glindzicz M, Nance WE, Liu XZ, Wistow G, Smith RJ, Griffith AJ, Wilcox ER, Friedman TB, Morell RJ. Bork JM, et al. Among authors: desmukh d. Am J Hum Genet. 2001 Jan;68(1):26-37. doi: 10.1086/316954. Epub 2000 Nov 21. Am J Hum Genet. 2001. PMID: 11090341 Free PMC article.
Long-living liposomes as potential drug carriers.
Desmukh DS, Bear WD, Wisniewski HM, Brockerhoff H. Desmukh DS, et al. Biochem Biophys Res Commun. 1978 May 15;82(1):328-34. doi: 10.1016/0006-291x(78)90613-7. Biochem Biophys Res Commun. 1978. PMID: 666842 No abstract available.