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Segawa disease with a novel heterozygous mutation in exon 5 of the GCH-1 gene (E183K)

✍ Scribed by T. Ikeda; K. Kanmura; Y. Kodama; K. Sawada; H. Nunoi; K. Hasegawa

Book ID: 113498641
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 174 KB
Volume: 31
Category: Article
ISSN: 0387-7604
DOI: 10.1016/j.braindev.2008.05.012

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