MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)
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| Description | scientific article published on 28 November 2018 |
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author: Miriam Schmidts Rose-Mary Boustany Valentina Stanley Umut Altunoglu Abolfazl Rad |
| Publication date | November 28, 2018 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |