Prenatal diagnosis of oculocutaneous albinism type II and novel mutations in two Chinese families.
- Published Article
- Publication Date
Jun 01, 2007
This is the first report of prenatal diagnosis performed in families with oculocutaneous albinism type II (OCA2). Also, this report reveals three novel mutations of the P gene.
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This record was last updated on 07/03/2016 and may not reflect the most current and accurate biomedical/scientific data available from NLM.
The corresponding record at NLM can be accessed at https://www.ncbi.nlm.nih.gov/pubmed/17385796