𝔖 Bobbio Scriptorium
✦   LIBER   ✦

CEP 290 MUTATION: A RARE CAUSE OF CHRONIC KIDNEY DISEASE


Book ID
122329496
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
143 KB
Volume
63
Category
Article
ISSN
0272-6386

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mutations of the CEP290 gene encoding a
✍ Valeska Frank; Anneke I. den Hollander; Nadina Ortiz BrΓΌchle; Marijke N. Zonneve πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 328 KB

## 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