Osteoporosis in lysinuric protein intolerance
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF00710296
Reference35 articles.
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3. Brody LC, Mitchell GA, Obie C et al (1992) Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.J Biol Chem 15: 3302?3307.
4. Carpenter TO, Levy HL, Holtrop ME, Shih VE, Anast CS (1985) Lysinuric protein intolerance presenting as childhood osteoporosis.N Engl J Med 31: 290?294.
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1. Lysinuric protein intolerance caused by a homozygous SLC7A7 deletion and presented with hyperferritinemia and osteoporosis in two siblings;Molecular Genetics and Metabolism Reports;2023-12
2. Delayed skeletal development and IGF-1 deficiency in a mouse model of lysinuric protein intolerance;Disease Models & Mechanisms;2023-08-01
3. It starts from the womb: maximizing bone health;Climacteric;2022-01-02
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5. Immune Dysregulation Mimicking Systemic Lupus Erythematosus in a Patient With Lysinuric Protein Intolerance: Case Report and Review of the Literature;Frontiers in Pediatrics;2021-05-20
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