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1.
Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly.
J Med Genet
; 57(4): 274-282, 2020 04.
Article
in English
| MEDLINE | ID: mdl-31586943
2.
Epidemiological evidence for a hereditary contribution to myasthenia gravis: a retrospective cohort study of patients from North America.
BMJ Open
; 10(9): e037909, 2020 09 18.
Article
in English
| MEDLINE | ID: mdl-32948566
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