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

Author:

Morris-Rosendahl DJ,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,Uyanik G

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference34 articles.

1. Genotypically defined lissencephalies show distinct pathologies;Forman;J Neuropathol Exp Neurol,2005

2. Developmental aspects of lissencephaly and the lissencephaly syndromes;Dobyns;Birth Defects Orig Artic Ser,1987

3. Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly;Dobyns;Am J Med Genet,1984

4. Clinical and molecular diagnosis of Miller-Dieker syndrome;Dobyns;Am J Hum Genet,1991

5. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats;Reiner;Nature,1993

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