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Mutation of a tubulin-specific chaperone, TBCE, causes the HRD/Sanjad-Sakati autosomal recessive Kenny-Caffey syndrome
- Authors :
- Diaz, Ga
Al Aqeel, A.
Gelb, Bd
Gordon, R.
Gorodischer, R.
Gregory, S.
Grossman, N.
Eli Hershkovitz
Kambouris, M.
Khan, Kts
Loeys, B.
Meyer, Bf
Mortier, G.
Parvari, R.
Sakati, N.
Sharony, R.
Weiner, R.
Zecic, A.
Hrd, Sanjad-Sakati Autosomal Recess
- Source :
- ResearcherID
Details
- Database :
- OpenAIRE
- Journal :
- ResearcherID
- Accession number :
- edsair.dedup.wf.001..488eaa954355d16c5c30b43468d5147d