Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter

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Abstract

Primary (or 'true') microcephaly is inherited as an autosomal recessive trait and is thought to be genetically heterogeneous. Using autozygosity mapping, we have identified a genetic locus (MCPH1) for primary microcephaly, at chromosome 8p22-pter, in two consanguineous families of Pakistani origin. Our results indicate that the gene lies within a 13-cM region between the markers D8S1824 and D8S1825 (maximum multipoint LOD score of 8.1 at D8S277). In addition, we have demonstrated the genetic heterogeneity of this condition by analyzing a total of nine consanguineous families with primary microcephaly.

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Jackson, A. P., McHale, D. P., Campbell, D. A., Jafri, H., Rashid, Y., Mannan, J., … Woods, C. G. (1998). Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter. American Journal of Human Genetics, 63(2), 541–546. https://doi.org/10.1086/301966

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