Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant
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| Title: | Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant |
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| Authors: | Gupta N; Vanderbilt University Medical Center, Department of Pediatrics, Division of Pediatric Endocrinology and Diabetes, Tennessee, USA; Mayo Clinic, Department of Pediatric and Adolescent Medicine, Division of Endocrinology and Metabolism, Minnesota, USA, Gregory SW; Mayo Clinic Health System, Department of Pediatric and Adolescent Medicine, Minnesota, USA, Deyle DR; Mayo Clinic, Department of Medical Genetics, Minnesota, USA, Tebben PJ; Mayo Clinic, Department of Pediatric and Adolescent Medicine, Division of Endocrinology and Metabolism, Minnesota, USA; Mayo Clinic, Department of Medicine, Division of Endocrinology, Metabolism and Nutrition, Minnesota, USA |
| Source: | Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2021 Jun 02; Vol. 13 (2), pp. 218-224. Date of Electronic Publication: 2020 Jun 10. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Galenos Yayınevi Country of Publication: Turkey NLM ID: 101519456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1308-5735 (Electronic) NLM ISO Abbreviation: J Clin Res Pediatr Endocrinol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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