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A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis.
Kirkgöz, Tarik; Özkan, Behzat; Hazan, Filiz; Acar, Sezer; Nalbantoglu, Özlem; Özkaya, Beyhan; Kulali, Melike Ataseven; Gürsoy, Semra; Ikegawa, Shiro; Guo, Long.
Affiliation
  • Kirkgöz T; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Özkan B; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Hazan F; Department of Medical Genetics, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Acar S; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Nalbantoglu Ö; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Özkaya B; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Kulali MA; Division of Pediatric Genetics, School of Medicine, Afyon Kocatepe University, Afyonkarahisar, Turkey.
  • Gürsoy S; Division of Pediatric Genetics, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Ikegawa S; Laboratory for Bone and Joint Diseases, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan.
  • Guo L; Laboratory for Bone and Joint Diseases, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan.
Front Genet ; 13: 938814, 2022.
Article in En | MEDLINE | ID: mdl-35812760
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Prognostic_studies Language: En Journal: Front Genet Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Prognostic_studies Language: En Journal: Front Genet Year: 2022 Document type: Article Affiliation country: Country of publication: