ATP13A2 novel mutations causing a rare form of...

Brain and Development 2018 / 6

ATP13A2 novel mutations causing a rare form of juvenile-onset Parkinson disease

Suleiman, Jehan, Hamwi, Nadia, El-Hattab, Ayman W.
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Language:
english
Journal:
Brain and Development
DOI:
10.1016/j.braindev.2018.05.017
Date:
June, 2018
File:
PDF, 190 KB
english, 2018
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