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- amino acid metabolism, inborn errors 4 Treffer
- carrier proteins 4 Treffer
- alleles 3 Treffer
- fusion regulatory protein 1, light chains 3 Treffer
- humans 3 Treffer
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40 weitere Werte:
- amino acid transport disorders, inborn 2 Treffer
- cell membrane 2 Treffer
- dna mutational analysis 2 Treffer
- exons 2 Treffer
- female 2 Treffer
- founder effect 2 Treffer
- male 2 Treffer
- membrane proteins 2 Treffer
- mutation 2 Treffer
- 5' untranslated regions 1 Treffer
- alternative splicing 1 Treffer
- amino acid transport system y+l 1 Treffer
- amino acid transport systems, basic 1 Treffer
- amino acids, diamino 1 Treffer
- aminoaciduria 1 Treffer
- animals 1 Treffer
- biology 1 Treffer
- dimerization 1 Treffer
- dogs 1 Treffer
- epithelial cells 1 Treffer
- exon 1 Treffer
- genetic carrier screening 1 Treffer
- genetics 1 Treffer
- genetics (clinical) 1 Treffer
- infant, newborn 1 Treffer
- introns 1 Treffer
- japan 1 Treffer
- kidney tubules 1 Treffer
- lysinuric protein intolerance 1 Treffer
- medicine 1 Treffer
- medicine.disease 1 Treffer
- mutant 1 Treffer
- mutation testing 1 Treffer
- oocytes 1 Treffer
- pedigree 1 Treffer
- protein structure, tertiary 1 Treffer
- renal aminoacidurias 1 Treffer
- rna splicing 1 Treffer
- transversion 1 Treffer
- xenopus laevis 1 Treffer
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In: Human mutation, Jg. 16 (2000-09-01), Heft 3, S. 270-1Online academicJournalZugriff:
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In: Human mutation, Jg. 16 (2000-09-12), Heft 3Online unknownZugriff:
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In: Human mutation, Jg. 29 (2008), Heft 1, S. 14-21Online academicJournalZugriff:
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In: Human mutation, Jg. 25 (2005-04-01), Heft 4, S. 410Online academicJournalZugriff:
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In: Human mutation, Jg. 15 (2000), Heft 4, S. 367-72Online academicJournalZugriff:
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In: Human mutation, Jg. 25 (2005-03-19), Heft 4Online unknownZugriff:
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SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance familiesIn: Human mutation, Jg. 15 (2000-03-29), Heft 4Online unknownZugriff: