Homozygous null mutations of ROR2 tyrosine kinase cause the autosomal recessive form of Robinow syndrome

Authors :: Brunner, H.G.
Celli, J.
Kayserili, H.
van Beusekom, E.
Brussel, W.
Skovby, F.
Kerr, B.
Balci, S.
Percin, E.F.
Akarsu, N.
van Bokhoven, H.
Source :: American Journal of Human Genetics. Oct, 2000, Vol. 67 Issue 4, 40
Publication Year :: 2000

Subjects :: Protein tyrosine kinase -- Genetic aspects
Gene mutations -- Research
Biological sciences

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