Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa

Li L., Jiao X., D’Atri I., Ono F., Nelson R., Chan C-C., Nakaya N., Ma Z., Ma Y., Cai X., Zhang L., Lin S., Hameed A., Chioza BA., Hardy H., Arno G., Hull S., Khan MI., Fasham J., Harlalka GV., Michaelides M., Moore AT., Coban Akdemir ZH., Jhangiani S., Lupski JR., Cremers FPM., Qamar R., Salman A., Chilton J., Self J., Ayyagari R., Kabir F., Naeem MA., Ali M., Akram J., Sieving PA., Riazuddin S., Baple EL., Riazuddin SA., Crosby AH., Hejtmancik JF.

DOI

10.1371/journal.pgen.1007504

Type

Journal article

Publisher

Public Library of Science (PLoS)

Publication Date

2018-08-29T00:00:00+00:00

Volume

14

Pages

e1007504 - e1007504

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