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Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy.
Eur J Hum Genet. 2015 Apr;23(4):473-80. doi: 10.1038/ejhg.2014.136. Epub 2014 Jul 23.
Eur J Hum Genet. 2015.
PMID: 25052312
Free PMC article.
Immortality of cell lines: challenges and advantages of establishment.
Maqsood MI, Matin MM, Bahrami AR, Ghasroldasht MM.
Maqsood MI, et al.
Cell Biol Int. 2013 Oct;37(10):1038-45. doi: 10.1002/cbin.10137. Epub 2013 Jun 24.
Cell Biol Int. 2013.
PMID: 23723166
Review.
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Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population.
Jaworek TJ, Kausar T, Bell SM, Tariq N, Maqsood MI, Sohail A, Ali M, Iqbal F, Rasool S, Riazuddin S, Shaikh RS, Ahmed ZM.
Jaworek TJ, et al. Among authors: maqsood mi.
Orphanet J Rare Dis. 2012 Jun 26;7:44. doi: 10.1186/1750-1172-7-44.
Orphanet J Rare Dis. 2012.
PMID: 22734612
Free PMC article.
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