Associated Papers
Majeed Syndrome: Five Cases With Novel Mutations From Unrelated Families in India With a Review of Literature.
Chavan PP et al.
The Journal of Rheumatology, 2021
Exome sequencing as the first-tier test for pediatric respiratory diseases: A single-center study.
Hao C et al.
Human Mutation, 2021
Novel Majeed Syndrome-Causing LPIN2 Mutations Link Bone Inflammation to Inflammatory M2 Macrophages and Accelerated Osteoclastogenesis.
Bhuyan F et al.
Arthritis & Rheumatology (hoboken, N.j.), 2021
Majeed Syndrome: A Review of the Clinical, Genetic and Immunologic Features.
Ferguson PJ et al.
Biomolecules, 2021
Compound heterozygous LPIN2 pathogenic variants in a patient with Majeed syndrome with recurrent fever and severe neutropenia: case report.
Liu J et al.
Bmc Medical Genetics, 2019
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