SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.
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| Title: | SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably. |
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| Authors: | Bukowska-Olech, Ewelina1 (AUTHOR) ewe.olech@gmail.com, Sowińska-Seidler, Anna1 (AUTHOR), Wierzba, Jolanta2 (AUTHOR), Jamsheer, Aleksander1,3 (AUTHOR) jamsheer@wp.pl |
| Source: | Orphanet Journal of Rare Diseases. 8/26/2022, Vol. 17 Issue 1, p1-8. 8p. |
| Database: | Academic Search Ultimate |
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| ISSN: | 17501172 |
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| DOI: | 10.1186/s13023-022-02480-w |
