Progress in Mapping Human Epilepsy Genes

Epilepsia

Volumn 35, Issue , 1994, Pages S29-S40

  Delgado‐Escueta, Antonio V ^a,b,c   Serratosa, Jose M ^a,b,c   Liu, Amy ^a,b,c   Weissbecker, Karen ^c   Medina, Marco T ^a,c,e   Gee, Manyee ^a,b   Treiman, Lucy J ^a,b,c   Sparkes, Robert S ^a,d  

^a Louisiana State University ^*  (United States)

^b LOUISIANA STATE UNIVERSITY   (United States)

^c LOUISIANA STATE UNIVERSITY   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e NATIONAL AUTONOMOUS UNIVERSITY OF HONDURAS   (Honduras)

Author keywords

Benign familial neonatal convulsion; Chromosome 6p; Epilepsy juvenile myoclonic 1; Gene mapping; Progressive myoclonic epilepsy

Indexed keywords

HLA ANTIGEN; HLA DQ ANTIGEN; LYSINE TRANSFER RNA; PROPERDIN;

ABSENCE; CHROMOSOME 10; CHROMOSOME 16P; CHROMOSOME 1Q; CHROMOSOME 20Q; CHROMOSOME 21Q; CHROMOSOME 22Q; CHROMOSOME 6P; CHROMOSOME 8Q; CHROMOSOME MAP; CONFERENCE PAPER; GAUCHER DISEASE; GENERALIZED EPILEPSY; GENETIC HETEROGENEITY; HUMAN; MYOCLONUS EPILEPSY; NEURONAL CEROID LIPOFUSCINOSIS; POINT MUTATION; PRIORITY JOURNAL; SIALIDOSIS;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 6; EPILEPSIES, MYOCLONIC; EPILEPSY; GENETIC MARKERS; HUMAN; LINKAGE (GENETICS); LOD SCORE; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0028082058     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1157.1994.tb05926.x     Document Type: Article

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