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M. Laura Duque Lasio
lduque@wustl.edu
phone:
Training
Combined Pediatrics and Medical Genetics Resident, St. Louis Children's Hospital
,
2015
-
2019
Medical Biochemical Genetics Fellow, UPMC Children's Hospital of Pittsburgh
,
2019
-
2020
Clinical Biochemical Genetics Fellow, University of Utah Health
,
2020
-
2022
Recent Publications
view all (4)
Publication Co-Authors
Sakil S Kulkarni, MD
Beth A. Kozel, M.D., Ph.D.
Janis M. Stoll, M.D.
Tomi L. Toler, MS, CGC
Lines MA, Cuillerier A, Chakraborty P, Naas T, Duque Lasio ML, Michaud J, Pileggi C, Harper ME, Burelle Y, Toler TL, Sondheimer N, Crawford HP, Millan F, Geraghty MT.
A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency.
Eur J Hum Genet
.
2021;29
(11):
1719-1724.
PMCID:
PMC8560863
PMID:
34483339
Guenzel AJ, Turgeon CT, Nickander KK, White AL, Peck DS, Pino GB, Studinski AL, Prasad VK, Kurtzberg J, Escolar ML, Lasio MLD, Pellegrino JE, Sakonju A, Hickey RE, Shallow NM, Ream MA, Orsini JJ, Gelb MH, Raymond K, Gavrilov DK, Oglesbee D, Rinaldo P, Tortorelli S, Matern D.
The critical role of psychosine in screening, diagnosis, and monitoring of Krabbe disease.
Genet Med
.
2020;22
(6):
1108-1118.
PMID:
32089546
Kulkarni S, Abro B, Duque Lasio ML, Stoll J, Grange DK, He M.
Clinical and Pathological Features of a Newborn With Compound Heterozygous
ANKS6
Variants.
Pediatr Dev Pathol
.
2020;23
(3):
235-239.
PMID:
31635528
Duque Lasio ML, Kozel BA.
Elastin-driven genetic diseases.
Matrix Biol
.
2018;71-72:144-160.
PMCID:
PMC8409172
PMID:
29501665
Last updated: 06/06/2022
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