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Refining the localization of the PKD2 locus on chromosome 4q by linkage analysis in Spanish families with autosomal dominant polycystic kidney disease type 2.

Autosomal dominant polycystic kidney disease (ADPKD) is a genetically heterogeneous disorder. At least two distinct forms of ADPKD are now well defined. In approximately 86% of affected European families, a gene defect localized to 16p13.3 was responsible for ADPKD, while a second locus has been rec...

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Detaylı Bibliyografya
Asıl Yazarlar: San Millán, J L, Viribay, M, Peral, B, Martínez, I, Weissenbach, J, Moreno, F
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1995
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801339/
https://ncbi.nlm.nih.gov/pubmed/7825585
Etiketler: Etiketle
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