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Paper Details

Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders.
NPJ Genom Med
8
2022
Author NameAffiliation
Anna HammarsjöKarolinska Institutet
Anna HammarsjöKarolinska University Hospital
Pengfei LiuBaylor College of Medicine
Pengfei Liu
Jennifer E PoseyBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital and Baylor College of Medicine
James R LupskiTexas Children's Hospital
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital and Baylor College of Medicine
James R LupskiTexas Children's Hospital
James R LupskiBaylor College of Medicine
Ann NordgrenKarolinska Institutet
Ann NordgrenKarolinska University Hospital
Giedre GrigelionieneKarolinska Institutet
Giedre GrigelionieneKarolinska University Hospital
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Release 1.2