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Author/Creator Lidov, Hart G. W.

2. Cover. Issue 3 (15th March 2019)

Authors:
Bruels, Christine C.; Li, Chengcheng; Mendoza, Tonatiuh; Khan, Jamillah; Reddy, Hemakumar M.; Estrella, Elicia A.; Ghosh, Partha S.; Darras, Basil T.; Lidov, Hart G. W.; Pacak, Christina A.; Kunkel, Louis M.; Modave, François; Draper, Isabelle; Kang, Peter B.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 3(2019)
Page Start:
i
Record Type:
Journal Article
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3. Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites. Issue 3 (28th January 2019)

Authors:
Bruels, Christine C.; Li, Chengcheng; Mendoza, Tonatiuh; Khan, Jamillah; Reddy, Hemakumar M.; Estrella, Elicia A.; Ghosh, Partha S.; Darras, Basil T.; Lidov, Hart G. W.; Pacak, Christina A.; Kunkel, Louis M.; Modave, François; Draper, Isabelle; Kang, Peter B.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 3(2019)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy. Issue 6 (16th May 2018)

Authors:
Winawer, Melodie R.; Griffin, Nicole G.; Samanamud, Jorge; Baugh, Evan H.; Rathakrishnan, Dinesh; Ramalingam, Senthilmurugan; Zagzag, David; Schevon, Catherine A.; Dugan, Patricia; Hegde, Manu; Sheth, Sameer A.; McKhann, Guy M.; Doyle, Werner K.; Grant, Gerald A.; Porter, Brenda E.; Mikati, Moham...
Journal:
Annals of neurology
Issue:
Volume 83:Issue 6(2018)
Page Start:
1133
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗