المؤلفون: Gu, Mian^1,2, Chen, Aiqun^1,2, Sun, Shubin^1,2, Xu, Guohua^1,2

المصدر: Molecular Plant (Cell Press). Mar2016, Vol. 9 Issue 3, p396-416. 21p.

مصطلحات موضوعية: *PHOSPHATE transport proteins, *GENETIC regulation in plants, *MOLECULAR genetics

المؤلفون: Williams, C. J., Zhang, Y., Timms, A., Bonavita, G., Caeiro, F., Broxholme, J., Cuthbertson, J., Jones, Y., Marchegiani, R., Reginato, A., Graham Russell, R., Wordsworth, B. P., Carr, A. J., Brown, Matthew A.

المصدر: American Journal of Human Genetics

مصطلحات موضوعية: ANKH protein, human, calcium pyrophosphate, membrane protein, phosphate transporter, amino acid sequence, article, chondrocalcinosis, chromosome 5, genetics, metabolic disorder, metabolism, molecular genetics, mutation, pedigree, sequence homology, Chromosomes, Pair 5, Humans, Membrane Proteins, Metabolic Diseases, Molecular Sequence Data, Phosphate Transport Proteins, Amino Acid

العلاقة: Williams, C. J., Zhang, Y., Timms, A., Bonavita, G., Caeiro, F., Broxholme, J., Cuthbertson, J., Jones, Y., Marchegiani, R., Reginato, A., Graham Russell, R., Wordsworth, B. P., Carr, A. J., & Brown, Matthew A. (2002) Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH. American Journal of Human Genetics, 71(4), pp. 985-991.; https://eprints.qut.edu.au/87702Test/; Institute of Health and Biomedical Innovation

الإتاحة: https://doi.org/10.1086/343053Test
https://eprints.qut.edu.au/87702Test/

المصدر: American Journal of Human Genetics

مصطلحات الفهرس: ANKH protein, human, calcium pyrophosphate, membrane protein, phosphate transporter, amino acid sequence, article, chondrocalcinosis, chromosome 5, genetics, metabolic disorder, metabolism, molecular genetics, mutation, pedigree, sequence homology, Chromosomes, Pair 5, Humans, Membrane Proteins, Metabolic Diseases, Molecular Sequence Data, Phosphate Transport Proteins, Amino Acid, Contribution to Journal

URL: doi:10.1086/343053
Williams, C. J., Zhang, Y., Timms, A., Bonavita, G., Caeiro, F., Broxholme, J., Cuthbertson, J., Jones, Y., Marchegiani, R., Reginato, A., Graham Russell, R., Wordsworth, B. P., Carr, A. J., & Brown, Matthew A. (2002) Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH. American Journal of Human Genetics, 71(4), pp. 985-991.