MYO5B, STX3 and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update
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| Description | scientific article published on 21 December 2017 |
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author: Anne Houdusse-Juillé Carsten Posovszky Herschel S Dhekne Sven C D van IJzendoorn Olena Pylypenko |
| Publication date | January 17, 2018 |
| Language | English |
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