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Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.

Aldave AJ, Yellore VS, Bourla N, Momi RS, Khan MA, Salem AK, Rayner SA, Glasgow BJ, Kurtz I.

Cornea. 2007 Aug;26(7):896-900.

PMID: 17667634 [PubMed - indexed for MEDLINE]

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