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Autor:
Anina, Bauer, John F, Bateman, Shireen R, Lamandé, Eric, Hanssen, Shannon G M, Kirejczyk, Mark, Yee, Ali, Ramiche, Vidyha, Jagannathan, Monika, Welle, Tosso, Leeb, Fiona L, Bateman
Publikováno v:
Genes
The Ehlers–Danlos syndromes (EDS) are a heterogeneous group of heritable disorders affecting connective tissues. The mutations causing the various forms of EDS in humans are well characterized, but the genetic mutations causing EDS-like clinical pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2704ec512fc83f628ffb43efa7922baa
https://pubmed.ncbi.nlm.nih.gov/31546637
https://pubmed.ncbi.nlm.nih.gov/31546637
Autor:
Eric Hanssen, V. Jagannathan, Anina Bauer, Ali Ramiche, Monika Maria Welle, Fiona L Bateman, Mark Yee, Shannon G.M. Kirejczyk, Shireen R. Lamandé, Tosso Leeb, John F. Bateman
BACKGROUNDThe Ehlers Danlos syndromes (EDS) are a heterogeneous group of heritable disorders affecting connective tissues. The mutations causing the various forms of EDS in humans are well characterized, but the genetic mutations causing EDS-like cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fe7e928dbf36b717e3f11ddded95c6a
https://doi.org/10.1101/660407
https://doi.org/10.1101/660407
Akademický článek
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Autor:
Ali Ramiche, V. Jagannathan, Fiona L Bateman, John F. Bateman, Shannon G.M. Kirejczyk, Monika Maria Welle, Eric Hanssen, Tosso Leeb, Shireen R. Lamandé, Mark Yee, Anina Bauer
Publikováno v:
Bauer, Anina; Bateman, John F; Lamandé, Shireen R; Hanssen, Eric; Kirejczyk, Shannon G M; Yee, Mark; Ramiche, Ali; Jagannathan, Vidya; Welle, Monika; Leeb, Tosso; Bateman, Fiona L (2019). Identification of Two Independent COL5A1 Variants in Dogs with Ehlers-Danlos Syndrome. Genes, 10(10) MDPI, Molecular Diversity Preservation International 10.3390/genes10100731
Genes, Vol 10, Iss 10, p 731 (2019)
Genes
Volume 10
Issue 10
Genes, Vol 10, Iss 10, p 731 (2019)
Genes
Volume 10
Issue 10
The Ehlers&ndash
Danlos syndromes (EDS) are a heterogeneous group of heritable disorders affecting connective tissues. The mutations causing the various forms of EDS in humans are well characterized, but the genetic mutations causing EDS-like cl
Danlos syndromes (EDS) are a heterogeneous group of heritable disorders affecting connective tissues. The mutations causing the various forms of EDS in humans are well characterized, but the genetic mutations causing EDS-like cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a947c70105c25c6476bd5d0df948950
https://doi.org/10.3390/genes10100731
https://doi.org/10.3390/genes10100731