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Partial albinism and immunodeficiency in patients with Hermansky-Pudlak Type II: Introducing 2 novel mutations.
Alizadeh, Zahra; Nabilou, Susan; Mazinani, Marzieh; Tajik, Shaghayegh; Hamidieh, Amir Ali; Houshmand, Masoud; Fazlollahi, Mohammad Reza; Pourpak, Zahra.
Affiliation
  • Alizadeh Z; Immunology, Asthma & Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Nabilou S; Immunology, Asthma & Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Mazinani M; Immunology, Asthma & Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Tajik S; Immunology, Asthma & Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Hamidieh AA; Pediatric Stem Cell Transplant Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Houshmand M; Department of Medical Genetics, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran.
  • Fazlollahi MR; Immunology, Asthma & Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Pourpak Z; Immunology, Asthma & Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Scand J Immunol ; 93(1): e12966, 2021 Jan.
Article de En | MEDLINE | ID: mdl-32869296

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Piébaldisme / Syndrome d'Hermanski-Pudlak / Complexe protéique adaptateur 3 / Complexe protéique adaptateur, sous-unités bêta / Lymphohistiocytose hémophagocytaire / Maladies d'immunodéficience primaire Limites: Adolescent / Child / Female / Humans / Male Langue: En Journal: Scand J Immunol Année: 2021 Type de document: Article Pays d'affiliation: Iran Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Piébaldisme / Syndrome d'Hermanski-Pudlak / Complexe protéique adaptateur 3 / Complexe protéique adaptateur, sous-unités bêta / Lymphohistiocytose hémophagocytaire / Maladies d'immunodéficience primaire Limites: Adolescent / Child / Female / Humans / Male Langue: En Journal: Scand J Immunol Année: 2021 Type de document: Article Pays d'affiliation: Iran Pays de publication: Royaume-Uni