DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Purnell SM, Bleyl SB, Bonkowsky JL.
Clinical exome sequencing identifies a novel TUBB4A mutation in a child with static hypomyelinating leukodystrophy.
Pediatr Neurol 2014;
50 (6) 608-611
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