Mutation in DHP receptor α1 subunit (CALCLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis
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| Veröffentlicht in: | Journal of medical genetics 1995, Vol.32 (1), p.44-47 |
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| container_title | Journal of medical genetics |
| container_volume | 32 |
| creator | BOERMAN, R. H OPHOFF, R. A FONTAINE, B PADBERG, G. W FRANTS, R. R LINKS, T. P VAN EIJK, R SANDRUIJL, L. A ELBAZ, A VALE-SANTOS, J. E WINTZEN, A. R VAN DEUTEKOM, J. C ISLES, D. E |
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| fulltext | fulltext |
| identifier | ISSN: 0022-2593 |
| ispartof | Journal of medical genetics, 1995, Vol.32 (1), p.44-47 |
| issn | 0022-2593 1468-6244 |
| language | eng |
| recordid | cdi_pascalfrancis_primary_3406892 |
| source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
| subjects | Biological and medical sciences Medical sciences Metabolic diseases Metals (hemochromatosis...) Other metabolic disorders |
| title | Mutation in DHP receptor α1 subunit (CALCLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis |
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