## Communicated by Iain McIntosh Meckel-Gruber syndrome (MKS) is an autosomal recessive, lethal multisystemic disorder characterized by meningooccipital encephalocele, cystic kidney dysplasia, hepatobiliary ductal plate malformation, and postaxial polydactyly. Recently, genes for MKS1 and MKS3 wer
β¦ LIBER β¦
Focus on Molecules: Centrosomal protein 290 (CEP290)
β Scribed by Phillip Moradi; Wayne L. Davies; Donna S. Mackay; Michael E. Cheetham; Anthony T. Moore
- Book ID
- 116457077
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 245 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0014-4835
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