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Paper Details

Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia.
EBioMedicine
5
2020
1, FYN, Integrin, LAMA5, LAMA5-, PYK2, RNA, SRC kinase, WNT, alpha-5, alpha-5 laminin basement membrane protein, bent bone dysplasia, bent bone skeletal disorder, cell signaling abnormalities, integrin, laminins, luciferase, skeletal disorder, skeletal disorders, vinculin
Author NameAffiliation
Michael J BamshadUniversity of Washington Center for Mendelian Genomics, University of Washington
Michael J BamshadUniversity of Washington Center for Mendelian Genomics, University of Washington
Deborah A NickersonUniversity of Washington Center for Mendelian Genomics, University of Washington
Deborah A NickersonUniversity of Washington Center for Mendelian Genomics, University of Washington
Jessica X ChongUniversity of Washington Center for Mendelian Genomics, University of Washington
Jessica X ChongUniversity of Washington Center for Mendelian Genomics, University of Washington
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