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A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter–Thompson type

Acromesomelic dysplasia is genetically heterogeneous group of skeletal disorders characterized by short stature and acromelia and mesomelia of limbs. Acromesomelic dysplasia segregates in an autosomal recessive pattern and is caused by biallelic sequence variants in three genes (NPR2, GDF5, and BMPR...

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Bibliographische Detailangaben
Veröffentlicht in:Ann Hum Genet
Hauptverfasser: Ullah, Asmat, Umair, Muhammad, Muhammad, Dost, Bilal, Muhammad, Lee, Kwanghyuk, Leal, Suzanne M, Ahmad, Wasim
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2018
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6141004/
https://ncbi.nlm.nih.gov/pubmed/29322508
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ahg.12233
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