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Genetic and Physical Mapping of the Locus for Autosomal Dominant Renal Fanconi Syndrome, on Chromosome 15q15.3

Autosomal dominant renal Fanconi syndrome is a genetic model for the study of proximal renal tubular transport pathology. We were able to map the locus for this disease to human chromosome 15q15.3 by genotyping a central Wisconsin pedigree with 10 affected individuals. After a whole-genome scan with...

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書誌詳細
主要な著者: Lichter-Konecki, U., Broman, K. W., Blau, E. B., Konecki, D. S.
フォーマット: Artigo
言語:Inglês
出版事項: The American Society of Human Genetics 2001
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1234925/
https://ncbi.nlm.nih.gov/pubmed/11090339
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