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 journalLetterpeer-review

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

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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