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Recurrent rhabdomyolysis in a patient with oculocutaneous albinism type 1 and platelet storage-pool deficiency. [electronic resource] by
- 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
Producer: 20081212
In:
American journal of medical genetics. Part A vol. 146A
Availability: No items available.
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