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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2 citations in Web of Science®

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ID Code: 89415
Item Type: Journal Article
Refereed: Yes
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
ISSN: 1015-8146
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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