Scott syndrome with novel compound heterozygous pathogenic variants in ANO6 and reduced thrombin generation.
- DOI
- 10.3324/haematol.2025.300111
- Published
- 2026 Aug 1
- Container
- Haematologica
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3324/haematol.2025.300111,
title = {Scott syndrome with novel compound heterozygous pathogenic variants in ANO6 and reduced thrombin generation.},
author = {Ahmed A and Montague SJ and Vyas H and Mistry J and Pavey NJ and Smith SRM and Griffith L and Clothier I and Hudson R and Faulkner E and Buka R and Bignell P and Fratter C and Marshall K and Bailiff B and Poulter NS and De Laat B and Huskens D and Lowe GC and Thomas SG and Morgan NV},
year = {2026},
journal = {Haematologica},
doi = {10.3324/haematol.2025.300111},
url = {https://doi.org/10.3324/haematol.2025.300111}
}RIS
TY - JOUR TI - Scott syndrome with novel compound heterozygous pathogenic variants in ANO6 and reduced thrombin generation. AU - Ahmed A AU - Montague SJ AU - Vyas H AU - Mistry J AU - Pavey NJ AU - Smith SRM AU - Griffith L AU - Clothier I AU - Hudson R AU - Faulkner E AU - Buka R AU - Bignell P AU - Fratter C AU - Marshall K AU - Bailiff B AU - Poulter NS AU - De Laat B AU - Huskens D AU - Lowe GC AU - Thomas SG AU - Morgan NV PY - 2026 JO - Haematologica DO - 10.3324/haematol.2025.300111 UR - https://doi.org/10.3324/haematol.2025.300111 ER -
APA
A, A., SJ, M., H, V., J, M., NJ, P., SRM, S., L, G., I, C., R, H., E, F., R, B., P, B., C, F., K, M., B, B., NS, P., B, D. L., D, H., GC, L., SG, T., & NV, M. (2026). Scott syndrome with novel compound heterozygous pathogenic variants in ANO6 and reduced thrombin generation.. Haematologica. https://doi.org/10.3324/haematol.2025.300111
Source records
- pubmed · retrieved 2026-09-26T17:15:57.818Z