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Clinical characteristics and family history of each patient screened for WFS1 mutations.

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Figshare2015-12-02 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_Clinical_characteristics_and_family_history_of_each_patient_screened_for_WFS1_mutations_/1167633
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*M, male; F, female; DM, diabetes mellitus; OA, optic atrophy; D, deafness; DI, diabetes insipidus, numbers indicate age at onset in years; +, symptomatic with unknown onset age; −, asymptomatic, Y; Yes, N; No, N/A; not applicable, □; consanguineous marriage and affected siblings.§Individual with detectable WFS1 mutation in single chromosome.Clinical characteristics and family history of each patient screened for WFS1 mutations.
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2015-12-02
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