Concepedia

Publication | Open Access

Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness

DOIFull Paper Access

195

Citations

50

References

2013

Year

Véronique Pingault, Virginie Bodereau, Viviane Baral, Séverine Marcos, Yuli Watanabe, Asma Chaoui, Corinne Fouveaut, Chrystel Leroy, O. Vérier‐Mine, Christine Francannet,
The American Journal of Human Genetics

References

YearCitations

Page 1