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Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of MUC5B.
Costain, Gregory; Liu, Zhen; Mennella, Vito; Radicioni, Giorgia; Goczi, Adrienn N; Albulescu, Alexandra; Walker, Susan; Ngan, Bo; Manson, David; Vali, Reza; Khan, Meraj; Palaniyar, Nades; Hill, David B; Hall, David A; Marshall, Christian R; Knowles, Michael; Zariwala, Maimoona A; Kesimer, Mehmet; Dell, Sharon D.
Afiliação
  • Costain G; Division of Clinical and Metabolic Genetics.
  • Liu Z; Genetics and Genome Biology, Research Institute.
  • Mennella V; Department of Paediatrics.
  • Radicioni G; Genetics and Genome Biology, Research Institute.
  • Goczi AN; Cell Biology Program.
  • Albulescu A; Biochemistry Department.
  • Walker S; Division of Life Science, The Hong Kong University of Science and Technology, Hong Kong, China.
  • Ngan B; Clinical & Experimental Sciences Academic Unit Biomedical Research Center, National Health Research Institute, University of Southampton, Southampton, United Kingdom.
  • Manson D; Marsico Lung Institute.
  • Vali R; Department of Pathology and Laboratory Medicine.
  • Khan M; Cell Biology Program.
  • Palaniyar N; Biochemistry Department.
  • Hill DB; Cell Biology Program.
  • Hall DA; Biochemistry Department.
  • Marshall CR; Genetics and Genome Biology, Research Institute.
  • Knowles M; The Centre for Applied Genomics.
  • Zariwala MA; Division of Pathology, Department of Paediatric Laboratory Medicine.
  • Kesimer M; Department of Diagnostic Imaging.
  • Dell SD; Department of Medical Imaging.
Am J Respir Crit Care Med ; 205(7): 761-768, 2022 04 01.
Article em En | MEDLINE | ID: mdl-35023825

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumopatias / Mucinas Limite: Adult / Animals / Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumopatias / Mucinas Limite: Adult / Animals / Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article