Concepedia

Publication | Open Access

Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia

DOIFull Paper Access

55

Citations

12

References

2012

Year

Céline Huber, Eissa Faqeih, Deborah Bartholdi, Christine Bôle‐Feysot, Zvi Borochowitz, Denise P. Cavalcanti, Amandine Frigo, Patrick Nitschké, J. Roume, Heloísa G. dos Santos,
The American Journal of Human Genetics

References

YearCitations

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