Published in
BMJ Publishing Group, Journal of Medical Genetics, 1(47), p. 8-21
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- ORCID
- ORCID
- BMJ Publishing Group
- [www.ncbi.nlm.nih.gov] | PDF
- [europepmc.org] | PDF
- [www.researchgate.net] | PDF
- [www.ncbi.nlm.nih.gov] | PDF
- [www.ncbi.nlm.nih.gov] | PDF
- [epub.ub.uni-muenchen.de] | PDF
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Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)
Journal article published in 2009 by
D. Doherty,
H. Özyurek,
M. A. Parisi,
L. S. Finn,
M. Gunay-Aygun,
M. Al-Mateen,
D. Bates,
C. Clericuzio,
H. Demir,
M. Dorschner,
A. J. van Essen,
W. A. Gahl,
M. Gentile 
,
N. T. Gorden,
A. Hikida
and other authors.
,
N. T. Gorden,
A. Hikida
and other authors.
This paper is available in a repository.
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