α-Thalassemia in Oraons—indigenous tribal population from Jharkhand, India: insights to common deletions

Human Genetics · Published 2026-07-30 · DOI 10.1007/s00439-026-02857-y

Authors (5)

Shaikh Roshan, Nadkarni Anita, Kerketta Lily, Ghosh Kanjaksha, Gorakshakar Ajit

Abstract

PubPorta does not have an abstract for this article yet.

Read the article at the publisher →

Publication details

Year

2026

Citation

Roshan, S., Anita, N., Lily, K., et al. (2026). α-Thalassemia in Oraons—indigenous tribal population from Jharkhand, India: insights to common deletions. Human Genetics. https://doi.org/10.1007/s00439-026-02857-y

Related articles

• Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome · Human Genetics · 2026 · Same journal
• Understanding the public’s intention to adopt CRISPR-Cas9: the effect of beliefs, knowledge, and innovativeness · Human Genetics · 2026 · Same journal
• Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot project · Human Genetics · 2026 · Same journal
• The involvement of TNFRSF25 in age-related hearing loss · Human Genetics · 2026 · Same journal
• Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes · Human Genetics · 2025 · Same journal
• Evaluating genetic-based disease prediction approaches through simulation · Human Genetics · 2026 · Same journal
• Exploratory analysis of HLA SNPs associated with occult HBV infection: a multicenter case–control study in Chinese blood donors · Human Genetics · 2025 · Same journal
• Identification of DNA methylation based prognostic subtype and signature in epithelial ovarian cancer · Human Genetics · 2025 · Same journal
• Age estimation of single nucleotide polymorphisms associated with autoinflammatory diseases in anatolia: insights from ancient and modern DNA · Human Genetics · 2025 · Same journal
• A homozygous synonymous variant in SMG5, encoding a nonsense-mediated mRNA decay factor, causes developmental delay with growth retardation and relative macrocephaly · Human Genetics · 2026 · Same journal