Refining the phenotype of α-1a Tubulin ( TUBA1A) mutation in patients with classical lissencephaly.

Published in:

Clinical Genetics, 2008, v. 74, n. 5, p. 425, doi. 10.1111/j.1399-0004.2008.01093.x

By:

• Morris-Rosendahl, D. J.;
• Najm, J.;
• Lachmeijer, A. M. A.;
• Sztriha, L.;
• Martins, M.;
• Kuechler, A.;
• Haug, V.;
• Zeschnigk, C.;
• Martin, P.;
• Santos, M.;
• Vasconcelos, C.;
• Omran, H.;
• Kraus, U.;
• Van der Knaap, M. S.;
• Schuierer, G.;
• Kutsche, K.;
• Uyanik, G.

Publication type:

Article