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Article

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

American journal of medical genetics. Part A - 1 Dec 2008

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

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Share to Adolescent
Share to Albinism, Oculocutaneous
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19006216
DOI: 10.1002/ajmg.a.32569
PMCID: PMC2615100

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