DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Fathallah DM, Bejaoui M, Sly WS, Lakhoua R, Dellagi K.
A unique mutation underlying carbonic anhydrase II deficiency syndrome in patients of Arab descent.
Hum Genet 1994;
94 (05) 581-582
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