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Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome).
- Source :
-
Clinical genetics [Clin Genet] 2013 Jan; Vol. 83 (1), pp. 92-5. Date of Electronic Publication: 2012 Apr 09. - Publication Year :
- 2013
- Subjects :
- Bone and Bones abnormalities
Bone and Bones physiopathology
Child
Cytoskeletal Proteins
Female
Hedgehog Proteins
Humans
Intracellular Signaling Peptides and Proteins
Mutation
Craniosynostoses genetics
Craniosynostoses physiopathology
Ectodermal Dysplasia genetics
Ectodermal Dysplasia physiopathology
Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1399-0004
- Volume :
- 83
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Clinical genetics
- Publication Type :
- Report
- Accession number :
- 22486404
- Full Text :
- https://doi.org/10.1111/j.1399-0004.2012.01880.x