Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation
<p>Abstract</p> <p>Background</p> <p>To identify the genetic defect associated with autosomal recessive congenital cataract (ARCC), mental retardation (MR) and ARCC, MR and microcephaly present in most patients in four Tunisian consanguineous families.</p> <p&g...
Main Authors: | Chograni Manèl, Chaabouni Myriam, Mâazoul Faouzi, Bouzid Hedi, Kraiem Abdelhafid, Chaabouni Habiba |
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Format: | Article |
Language: | English |
Published: |
BMC
2011-11-01
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Series: | BMC Ophthalmology |
Online Access: | http://www.biomedcentral.com/1471-2415/11/35 |
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