Annals of Hematology

, Volume 89, Issue 10, pp 1057–1059

MYH9-related disease: Report on five German families and description of a novel mutation

  • Anna Savoia
  • Manuela Germeshausen
  • Daniela De Rocco
  • Bettina Henschel
  • Christian P. Kratz
  • Michaela Kuhlen
  • Bettina Rath
  • Klaus-Peter Steuhl
  • Cornelia Wermes
  • Matthias Ballmaier
Letter to the Editor

DOI: 10.1007/s00277-010-0928-y

Cite this article as:
Savoia, A., Germeshausen, M., De Rocco, D. et al. Ann Hematol (2010) 89: 1057. doi:10.1007/s00277-010-0928-y

Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  • Anna Savoia
    • 1
  • Manuela Germeshausen
    • 2
  • Daniela De Rocco
    • 1
  • Bettina Henschel
    • 3
  • Christian P. Kratz
    • 4
  • Michaela Kuhlen
    • 5
  • Bettina Rath
    • 6
  • Klaus-Peter Steuhl
    • 7
  • Cornelia Wermes
    • 2
  • Matthias Ballmaier
    • 2
  1. 1.Medical Genetics, Department of Reproductive and Developmental Sciences, Institute for Maternal and Child Health, IRCCS “Burlo Garofolo”University of TriesteTriesteItaly
  2. 2.Department of Pediatric Hematology and OncologyHannover Medical SchoolHannoverGermany
  3. 3.Marienhospital GelsenkirchenGelsenkirchenGermany
  4. 4.Department of Pediatrics and Adolescent MedicineUniversity of FreiburgFreiburgGermany
  5. 5.Clinic of Pediatric Oncology, Hematology and Clinical ImmunologyCenter for Child and Adolescent Health, Heinrich-Heine-UniversityDüsseldorfGermany
  6. 6.Department of Pediatric Hematology-OncologyUniversity of MünsterMünsterGermany
  7. 7.Clinic for Diseases of the Anterior Segments of the EyesEssen University HospitalEssenGermany

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