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A Novel Frameshift Mutation in Exon 23 of ATP7A (MNK) Results in Occipital Horn Syndrome and Not in Menkes Disease

✍ Scribed by Susan L. Dagenais; Ayla N. Adam; Jeffrey W. Innis; Thomas W. Glover

Book ID: 117853656
Publisher: American Society of Human Genetics
Year: 2001
Tongue: English
Weight: 580 KB
Volume: 69
Category: Article
ISSN: 0002-9297
DOI: 10.1086/321290

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