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Mandibuloacral Dysplasia Type a Lipodystrophy
A mandibuloacral dysplasia that is caused by homozygous or compound heterozygous mutation in the gene encoding lamin A/C (LMNA) on chromosome 1q22 and that is characterized by growth retardation, craniofacial anomalies w
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Overview
A mandibuloacral dysplasia that is caused by homozygous or compound heterozygous mutation in the gene encoding lamin A/C (LMNA) on chromosome 1q22 and that is characterized by growth retardation, craniofacial anomalies w
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