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Oculocutaneous albinism type 2 with a P gene missense mutation in a patient with Angelman syndrome
- Dr Saitoh, ss11{at}med.hokudai.ac.jp
Citation
Oculocutaneous albinism type 2 with a P gene missense mutation in a patient with Angelman syndrome
Publication history
- First published May 1, 2000.
Online issue publication
April 27, 2016
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Journal of Medical Genetics