Scott syndrome with novel compound heterozygous pathogenic variants in ANO6 and reduced thrombin generation.

Ahmed A, Montague SJ, Vyas H, Mistry J, Pavey NJ, Smith SRM, Griffith L, Clothier I, Hudson R, Faulkner E, Buka R, Bignell P, Fratter C, Marshall K, Bailiff B, Poulter NS, De Laat B, Huskens D, Lowe GC, Thomas SG, Morgan NV

Open source

DOI
10.3324/haematol.2025.300111
Published
2026 Aug 1
Container
Haematologica
Publisher
Not recorded
Open access
yes

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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

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