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Quinn, Lori ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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Milton, Rebecca, Gillespie, David, Dyer, Calie, Taiyari, Khadijeh, Carvalho, Maria J, Thomson, Kathryn, Sands, Kirsty, Portal, Edward A.R., Hood, Kerenza ![]() ![]() ![]() ![]() |
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Allen, Davina ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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Allen, Davina ![]() ![]() ![]() ![]() ![]() ![]() |
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D'Amore, Simona, Page, Kathleen, Donald, Aimée, Taiyari, Khadijeh, Tom, Brian, Deegan, Patrick, Tan, Chong Y., Poole, Kenneth, Jones, Simon A., Mehta, Atul, Hughes, Derralynn, Sharma, Reena, Lachmann, Robin H., Chakrapani, Anupam, Geberhiwot, Tarekegn, Santra, Saikat, Banka, Siddarth, Cox, Timothy M., Cox, T. M., Platt, F. M., Banka, S., Chakrapani, A., Deegan, P. B., Geberhiwot, T., Hughes, D. A., Jones, S., Lachmann, R. H., Santra, S., Sharma, R. and Vellodi, A.
2021.
In-depth phenotyping for clinical stratification of Gaucher disease.
Orphanet Journal of Rare Diseases
16
(1)
, 431.
10.1186/s13023-021-02034-6
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Sands, Kirsty, Carvalho, Maria J., Portal, Edward, Thomson, Kathryn, Dyer, Calie, Akpulu, Chinenye, Andrews, Robert, Ferreira, Ana, Gillespie, David ![]() ![]() ![]() ![]() |
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