The detection of carriers in hereditary myoclonic epilepsy
Acta Genet Med Gemellol (Roma)
.
1960 Oct:9:466-71.
doi: 10.1017/s1120962300018199.
Authors
M B SARLIN
,
H W KLOEPFER
,
W A MICKLE
,
R G HEATH
PMID:
13746547
DOI:
10.1017/s1120962300018199
No abstract available
MeSH terms
Epilepsies, Myoclonic*
Epilepsy / genetics*
Heterozygote*
Humans