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Kumarie Latchman
Kumarie Latchman
University of Miami
Medicine
Pediatrics
Neurodevelopmental disorder
Genetics
Biology
5
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2
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0
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AVPR2-related nephrogenic syndrome of inappropriate antidiuresis in four African American brothers
2021
Molecular Genetics and Metabolism
Michael Saad-Naguib
Kumarie Latchman
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A founder non-coding GALT variant interfering with splicing causes galactosemia.
2020
Journal of Inherited Metabolic Disease
Kumarie Latchman
Jeanette Brown
Claire J. Sineni
Lorrien Ragin‐Dames
Shengru Guo
Jingyu Huang
Willa Thorson
Stephanie Hacker
Deborah Barbouth
Mustafa Tekin
Guney Bademci
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Autosomal dominant inheritance in a recently described ZMIZ1‐related neurodevelopmental disorder: Case report of siblings and an affected parent
2019
American Journal of Medical Genetics Part A
Kumarie Latchman
Madison Calder
Dayna Morel
Lindsay Rhodes
Jane Juusola
Mustafa Tekin
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Spastic Diplegia in a Haitian Girl with Angelman Syndrome
2019
Journal of pediatric genetics
Kumarie Latchman
Margarita Nieto-Moreno
Roberto Lopez-Alberola
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Labyrinthine aplasia, microtia, and microdontia (LAMM) syndrome and FGF3 mutations
2013
Kumarie Latchman
Mustafa Tekin
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