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Publication | Open Access

Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3

DOIFull Paper Access

33

Citations

17

References

2017

Year

Muhammad Umair, Bader Alhaddad, Afzal Rafique, Abid Jan, Tobias B. Haack, Elisabeth Graf, Asmat Ullah, Farooq Ahmad, Tim M. Strom, Thomas Meitinger,
Pediatric Research

References

YearCitations

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