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4039089
4039089
https://w3id.org/oc/corpus/br/4039089
A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease
P3181
95ec7d8c904d94c7b42c9e5a2a53fa2a16a682bb
P3181
Q28367963-EC494536-AC0F-442A-8571-45CB1EFF773E
P3181
4039089
https://w3id.org/oc/corpus/br/4039089