Response to "mutations of the Noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al


Autoria(s): 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.
Data(s)

2008

Identificador

http://eprints.qut.edu.au/89415/

Publicador

Editions Medecine et Hygiene

Relação

http://www.ncbi.nlm.nih.gov/pubmed/18990993

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.

Fonte

Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #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
Tipo

Journal Article