Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiency

Despina Contopoulos-Ioannidis, Athanasios Evangeliou, Henk Ter Laak, Bert De Vries, Rolph Pfundt, Hans Scheffer, Jan Smeitink, Meropi Tzoufi, Alexandros Makis, Evangelos Marinos, Richard Hess, David Adams, Marjan Huizing, Eva Morava

Research output: Contribution to journalLetter

Original languageEnglish (US)
Pages (from-to)3100-3103
Number of pages4
JournalAmerican Journal of Medical Genetics, Part A
Volume146
Issue number23
DOIs
StatePublished - Dec 1 2008

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Contopoulos-Ioannidis, D., Evangeliou, A., Ter Laak, H., De Vries, B., Pfundt, R., Scheffer, H., Smeitink, J., Tzoufi, M., Makis, A., Marinos, E., Hess, R., Adams, D., Huizing, M., & Morava, E. (2008). Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiency. American Journal of Medical Genetics, Part A, 146(23), 3100-3103. https://doi.org/10.1002/ajmg.a.32569