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Results of search for 'au:"Almannai, M"'
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Authors
Al Mutairi, F
AlWadei, A H
Alasmari, A
Aljadhai, Y I
Alkuraya, F S
Almannai, M
Alotaibi, M
Alqasmi, A
Craigen, W
Eyaid, W
Faqeih, E
Faqeih, E A
Saleh, M M
Samman, M M
Shamseldin, H E
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Acidosis, Lactic
Adolescent
Adult
Alleles
Cerebellum
Child
Child, Preschool
DNA, Mitochondrial
Dandy-Walker Syndrome
Exome Sequencing
Female
Genetic Predisposition to Disease
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Loss of Function Mutation
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Mitochondria
Phenotype
genetics
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English
Your search returned 2 results.
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1.
Phenotypic characterization of KCTD3-related developmental epileptic encephalopathy.
[electronic resource]
by
Faqeih, E A
Almannai, M
Saleh, M M
AlWadei, A H
Samman, M M
Alkuraya, F S
Producer:
20190925
In:
Clinical genetics
vol. 93
Online resources:
Available from publisher's website
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No items available.
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2.
Expanding the phenotype of SLC25A42-associated mitochondrial encephalomyopathy.
[electronic resource]
by
Almannai, M
Alasmari, A
Alqasmi, A
Faqeih, E
Al Mutairi, F
Alotaibi, M
Samman, M M
Eyaid, W
Aljadhai, Y I
Shamseldin, H E
Craigen, W
Alkuraya, F S
Producer:
20190925
In:
Clinical genetics
vol. 93
Online resources:
Available from publisher's website
Availability:
No items available.
Save to lists
Add to cart
(remove)