| scholarly article | Q13442814 |
| P356 | DOI | 10.1136/JMG.28.4.241 |
| P953 | full work available at URL | https://europepmc.org/articles/PMC1016824 |
| https://europepmc.org/articles/PMC1016824?pdf=render | ||
| https://syndication.highwire.org/content/doi/10.1136/jmg.28.4.241 | ||
| P932 | PMC publication ID | 1016824 |
| P698 | PubMed publication ID | 1856829 |
| P5875 | ResearchGate publication ID | 21298813 |
| P50 | author | Nicholas Cross | Q42628914 |
| P2093 | author name string | G. Sebastio | |
| G. Andria | |||
| T. M. Cox | |||
| R. Gatti | |||
| P. Strisciuglio | |||
| R. de Franchis | |||
| C. Dionisi Vici | |||
| G. Sabetta | |||
| P2860 | cites work | Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation | Q24298317 |
| Complete amino acid sequence for human aldolase B derived from cDNA and genomic clones | Q24596462 | ||
| A new aldolase B variant, N334K, is a common cause of hereditary fructose intolerance in Yugoslavia | Q24615774 | ||
| Isolation and nucleotide sequence of a full-length cDNA coding for aldolase B from human liver | Q24634399 | ||
| Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia | Q27861076 | ||
| Molecular analysis of aldolase B genes in hereditary fructose intolerance | Q28254811 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Italy | Q38 |
| genetics | Q7162 | ||
| P304 | page(s) | 241-243 | |
| P577 | publication date | 1991-04-01 | |
| P1433 | published in | Journal of Medical Genetics | Q14640281 |
| P1476 | title | Aldolase B mutations in Italian families affected by hereditary fructose intolerance | |
| P478 | volume | 28 |
| Q35194185 | Association of the widespread A149P hereditary fructose intolerance mutation with newly identified sequence polymorphisms in the aldolase B gene |
| Q28638020 | Hereditary fructose intolerance |
| Q36571546 | Hereditary fructose intolerance in Brazilian patients |
| Q41885794 | Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population |
| Q41809721 | Integration of PCR-Sequencing Analysis with Multiplex Ligation-Dependent Probe Amplification for Diagnosis of Hereditary Fructose Intolerance. |
| Q28271637 | Molecular basis of hereditary fructose intolerance: mutations and polymorphisms in the human aldolase B gene |
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