Response to "mutations of the Noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al
Kaplan, F.S., Xu, M., Feldman, G., Brown, M.A., Cho, T.J., Choi, I.H., Connor, J.M., Longo Ribeiro Delai, P., Economides, A.N., Glaser, D.L., Groppe, J., Katagiri, T., Le Merrer, M., Morhart, R., Ravazzolo, R., Rogers, J.G., Smith, R., Triffitt, J.T., Urtizberea, J.A., Zasloff, M., & Shore, E.M. (2008) Response to "mutations of the Noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al. Genetic Counseling, 19(3), pp. 357-359.
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|Item Type:||Journal Article|
|Keywords:||activin A receptor 1, amino acid, bone morphogenetic protein receptor 1, glycine, noggin, serine, unclassified drug, amino acid sequence, amino acid substitution, chromosome 2q, gene mapping, gene mutation, genetic linkage, heterozygosity, human, letter, missense mutation, ossifying myositis, phenotype, polymerase chain reaction, protein function, single nucleotide polymorphism, Activin Receptors, Type I, Alleles, Carrier Proteins, Chromosome Mapping, Chromosomes, Human, Pair 2, DNA Mutational Analysis, Heterozygote Detection, Humans, Mutation, Missense, Myositis Ossificans, Predictive Value of Tests, Terminology as Topic|
|Divisions:||Current > QUT Faculties and Divisions > Faculty of Health
Current > Institutes > Institute of Health and Biomedical Innovation
|Deposited On:||23 Oct 2015 03:34|
|Last Modified:||23 Aug 2016 00:00|
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