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Browsing by Author Khanna, H.

Full Text	Issue Date	Title	Author(s)
	2010	Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy.	Otto, E.A.; Hurd, T.W.; Airik, R., et al
	2009	A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.	Khanna, H.; Davis, E.E.; Murga-Zamalloa, C.A., et al
	2010	Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.	O'Toole, J.F.; Liu, Y.; Davis, E.E., et al