Recurrent rhabdomyolysis in a patient with oculocutaneous...

American Journal of Medical Genetics Part A 2008 Vol. 146A; Iss. 23

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 A
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Volume:
146A
Year:
2008
Language:
english
Pages:
4
DOI:
10.1002/ajmg.a.32569
File:
PDF, 127 KB
english, 2008
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