Whole-exome sequencing identifies mutations in in a mild form of Carey-Fineman-Ziter syndrome.
Neurol Genet
| Authors | |
| Year of Publication | 2018
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| Journal | Neurol Genet
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| Volume | 4
|
| Issue | 2
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| Pages | e226
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| Date Published | 2018 Apr
|
| ISSN | 2376-7839
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| DOI | 10.1212/NXG.0000000000000226
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| PubMed ID | 29560417
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| PubMed Central ID | PMC5858950
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| Links | |
| Grant list | UM1 HG008900 / HG / NHGRI NIH HHS / United States
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