Mutation in DHP receptor alpha1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis
Publication year
1995Source
Journal of Medical Genetics, 32, 1, (1995), pp. 44-47ISSN
Publication type
Article / Letter to editor

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Organization
Nijmeegs Instituut voor Missiologie (NIM)
Journal title
Journal of Medical Genetics
Volume
vol. 32
Issue
iss. 1
Page start
p. 44
Page end
p. 47
This item appears in the following Collection(s)
- Academic publications [202606]
- Electronic publications [100803]
- Faculty of Philosophy, Theology and Religious Studies [10868]
- Open Access publications [69538]
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