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, Najm, J, Lachmeijer, AMA, Sztriha, L, Martins, M, Kuechler, A, Haug, V, Zeschnigk, C, Martin, P, Santos, M, Vasconcelos, C
, Omran, H, Kraus, U, Van der Knaap, MS, Schuierer, G, Kutsche, K and Uyanik, G
(2008)
Refining the phenotype of α‐1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly.
Clinical Genetics 74 (5), pp. 425-433.
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