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Homozygous deletion of exons 2 and 3 of NPC2 associated with Niemann-Pick disease type C.
Am J Med Genet A. 2016 Sep;170(9):2486-9. doi: 10.1002/ajmg.a.37794. Epub 2016 Jun 8.
Am J Med Genet A. 2016.
PMID: 27271431
Free PMC article.
No abstract available.
Myelodysplastic syndrome with multilineage dysplasia evolving to acute myeloid leukemia: Noonan syndrome with c.218C>T mutation in PTPN11 gene.
Shenoy RD, Yeshvanth SK, Prasada L H, Shenoy V, Shetty V.
Shenoy RD, et al. Among authors: prasada l h.
Pediatr Blood Cancer. 2019 Feb;66(2):e27527. doi: 10.1002/pbc.27527. Epub 2018 Oct 30.
Pediatr Blood Cancer. 2019.
PMID: 30378271
No abstract available.
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Genomics of iron refractory iron deficiency anemia phenotype reveals a spectrum of novel pathogenic biallelic and monoallelic TMPRSS6 variants and rare overlapping disorders.
Sharma P, Bhatia P, Singh M, Das R, Attri SV, Ghara N, Prasada LH, Trehan A.
Sharma P, et al.
Gene. 2024 Feb 15;895:147981. doi: 10.1016/j.gene.2023.147981. Epub 2023 Nov 10.
Gene. 2024.
PMID: 37951373
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