SLC13A5 is the second gene associated with Kohlschütter-Tönz syndrome. [electronic resource]
Producer: 20171101Description: 54-62 p. digitalISSN:- 1468-6244
- Alleles
- Amelogenesis Imperfecta -- genetics
- Brain Diseases -- genetics
- Cohort Studies
- Dementia -- genetics
- Epilepsy -- genetics
- Exome -- genetics
- Female
- Genetic Linkage -- genetics
- Genetic Predisposition to Disease -- genetics
- Humans
- Male
- Membrane Proteins -- genetics
- Mutation -- genetics
- Nuclear Proteins -- genetics
- Pedigree
- Symporters -- genetics
- Tooth
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Publication Type: Clinical Trial; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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