UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly
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Published:2021-09
Issue:9
Volume:23
Page:1624-1635
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
Schnur Rhonda E.,
Yousaf Sairah,
Liu James,
Chung Wendy K.,
Rhodes Lindsay,
Marble Michael,
Zambrano Regina M.,
Sobreira Nara,
Jayakar Parul,
Pierpont Mary Ella,
Schultz Matthew J.,
Pichurin Pavel N.,
Olson Rory J.,
Graham Gail E.,
Osmond Matthew,
Contreras-García Gustavo A.,
Campo-Neira Karina A.,
Peñaloza-Mantilla Camilo A.,
Flage Mark,
Kuppa Srikar,
Navarro Karina,
Sacoto Maria J. Guillen,
Wentzensen Ingrid M.,
Scarano Maria I.,
Juusola Jane,
Prada Carlos E.,
Hufnagel Robert B.ORCID
Subject
Genetics (clinical)
Cited by
8 articles.
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