DavidHolmesMortonMD

Physician

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Office
535 Bunker Hill Rd
Strasburg, PA 17579
Phone+1 717-687-9407

Fax+1 717-687-9237

Children's Hospital of PhiladelphiaResidency, Pediatrics, 1986 - 1989
Boston Children’s Hospital/Boston Medical CenterResidency, Pediatrics, 1983 - 1986
Harvard Medical SchoolClass of 1983

PubMed

208 citations
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.
Victoria E.H. Carlton, Baruch Z. Harris, Erik G. Puffenberger, Ashok K. Batta, A. S. Knisely
Nature Genetics. 2003-05-01
471 citations
Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2
Kevin A. Strauss, Erik G. Puffenberger, Matthew J. Huentelman, Steven Gottlieb, Seth E. Dobrin
The New England Journal of Medicine. 2006-03-30
151 citations
Human ITCH E3 Ubiquitin Ligase Deficiency Causes Syndromic Multisystem Autoimmune Disease
Naomi J. Lohr, Jean P. Molleston, Kevin A. Strauss, Wilfredo Torres-Martinez, Eric A. Sherman
American Journal of Human Genetics. 2010-03-12

Abstracts/Posters

Pyruvate Kinase (PK) Protein and Enzyme Levels in the Diagnosis and Clinical Phenotype of PK Deficiency
D Holmes Morton, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/9/2019