Concepedia

Publication | Closed Access

A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment

DOI

19

Citations

39

References

2018

Year

Isabelle Schrauwen, Imen Chakchouk, Khurram Liaqat, Abid Jan, Shabir Hussain, Deborah A. Nickerson, Michael J. Bamshad, Asmat Ullah, Wasim Ahmad, Suzanne M. Leal
Human Genetics

References

YearCitations

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