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Sabrya Carim
Sabrya Carim
Manchester Academic Health Science Centre
Minor allele frequency
Connective tissue disease
Missense mutation
GDF6
Myhre syndrome
2
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20
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Investigating the role of IPIP27 in cell division
2017
Sabrya Carim
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Leri’s pleonosteosis, a congenital rheumatic disease, results from microduplication at 8q22.1 encompassing GDF6 and SDC2 and provides insight into systemic sclerosis pathogenesis
2015
Annals of the Rheumatic Diseases
Siddharth Banka
Stuart A. Cain
Sabrya Carim
Sarah B. Daly
Jill Urquhart
Günhan Erdem
Jade Harris
Michelle Bottomley
Dian Donnai
Bronwyn Kerr
Helen Kingston
Andreas Superti-Furga
Sheila Unger
Holly Ennis
Jane Worthington
Ariane L. Herrick
Catherine L. R. Merry
W.W. Yue
Cay M. Kielty
William G. Newman
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Citations (20)
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