Your browser doesn't support javascript.
loading
Oculocutaneous albinism and bleeding diathesis due to a novel deletion in the HPS3 gene.
Marek-Yagel, Dina; Abudi-Sinreich, Shachar; Macarov, Michal; Veber, Alvit; Shalva, Nechama; Philosoph, Amit Mary; Pode-Shakked, Ben; Malicdan, May Christine V; Anikster, Yair.
Afiliação
  • Marek-Yagel D; Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Tel-Hahsomer, Israel.
  • Abudi-Sinreich S; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Macarov M; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Veber A; Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD, United States.
  • Shalva N; Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
  • Philosoph AM; Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Tel-Hahsomer, Israel.
  • Pode-Shakked B; Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Tel-Hahsomer, Israel.
  • Malicdan MCV; Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Tel-Hahsomer, Israel.
  • Anikster Y; Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Tel-Hahsomer, Israel.
Front Genet ; 13: 936064, 2022.
Article em En | MEDLINE | ID: mdl-36046236

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article