Analysis of deletions in three McLeod patients: exclusion of…
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- DOI 10.1046/j.1365-2370.2000.00188.x
- PMID https://pubmed.ncbi.nlm.nih.gov/10651848
- OpenAlex ID W2083531428
- Type Article
- Language EN
- Published 01 Feb 2000
- Volume 27 (1)
- Pages 29–33
- Source European Journal of Immunogenetics
- Publisher Wiley
- FWCI 0.70
- Countries 1
- Institutions 2
- Added 24 Jun 2016
- Updated 16 Oct 2026
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Analysis of deletions in three McLeod patients: exclusion of the XS locus from the Xp21.1–Xp21.2 region
Article 2000 EN
The McLeod syndrome is a rare X-linked recessive disorder characterized by blood group, neuromuscular and haematopoietic abnormalities. It is caused by XK gene defects and may include large deletions in the Xp21 region. Analysis of three unrelated McLeod patients for the presence of the XK, DMD, CYBB, ETX1, RPGR and OTC loci, as well as for the DXS709 marker, revealed deletions from the 39th exon…
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6 authors| # | Author | Institutions | ORCID |
|---|---|---|---|
| 1 | Wassim El Nemer Corresponding | Inserm (FR) Institut National de la Transf… (FR) | |
| 2 | Yves Colin | Inserm (FR) Institut National de la Transf… (FR) | |
| 3 | Emmanuel Collec | Inserm (FR) Institut National de la Transf… (FR) | — |
| 4 | Pierre Gane | Inserm (FR) Institut National de la Transf… (FR) | — |
| 5 | Jean‐Pierre Cartron | Inserm (FR) Institut National de la Transf… (FR) | |
| 6 | Caroline Le Van Kim | Inserm (FR) Institut National de la Transf… (FR) |
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