reference/20770130

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/20770130

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endingPage	433
issn	1399-0004 0009-9163
issueIdentifier	5
pageRange	425-433
publicationName	Clinical Genetics
startingPage	425
bibliographicCitation	Morris‐Rosendahl D, Najm J, Lachmeijer 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, Schuierer G, Kutsche K, Uyanik G. Refining the phenotype of α‐1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly. Clinical Genetics. 2008 Oct 13;74(5):425–33. doi: 10.1111/j.1399-0004.2008.01093.x.
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date	2008-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1111/j.1399-0004.2008.01093.x https://pubmed.ncbi.nlm.nih.gov/18954413
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Refining the phenotype of α‐1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly
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