## Abstract Craniometaphyseal dysplasia is caused by mutations in __ANKH__ (ankylosis, progressive homolog [mouse]) in the majority of cases, and all of the reported mutations are single amino acid changes. Genomic DNA from an affected patient, his biological parents, and a sibling was amplified an
Craniometaphyseal dysplasia and chondrocalcinosis cosegregating in a family with an ANKH mutation
β Scribed by Gareth Baynam; Jack Goldblatt; Lyn Schofield
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 101 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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