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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

✍ Scribed by Walsh, Christopher A.; Hong, Susan E.; Shugart, Yin Yao; Huang, David T.; Shahwan, Saad Al; Grant, P. Ellen; Hourihane, Jonathan O'B.; Martin, Neil D.T.

Book ID: 109828894
Publisher: Nature Publishing Group
Year: 2000
Tongue: English
Weight: 361 KB
Volume: 26
Category: Article
ISSN: 1061-4036
DOI: 10.1038/79246

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