IMEN CHAKCHOUK to Sequence Analysis, DNA
This is a "connection" page, showing publications IMEN CHAKCHOUK has written about Sequence Analysis, DNA.
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Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53. Mol Genet Genomics. 2015 Aug; 290(4):1327-34.
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Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa. Invest Ophthalmol Vis Sci. 2018 09 04; 59(11):4552-4557.
Score: 0.025