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poor muscle tone
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Genetic Markers
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CTBP1
SYT1
PIGA
CCDC174
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Pathway Enrichment
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LEIN_NEURON_MARKERS
mitotic spindle
MODULE_486
AGGAAGC_MIR5163P
C2 domain
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Curated Studies
Most Correlated Studies
OMIM - Alazami-Yuan syndrome
OMIM - Baker-Gordon syndrome
OMIM - Shashi-Pena syndrome
OMIM - Muscle finding
OMIM - Multiple congenital anomalies
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Literature
Most Relevant Literature
Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectu…
Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder character…
Progressive spastic tetraplegia and axial hypotonia (STAHP) due to SOD1 deficiency: is it really a n…
Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephaly.
A novel nonsense variant in the NFE2L1 transcription factor in a patient with developmental delay, h…
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Clinical Trials
Most Relevant Clinical Trials
Muscle Tone Change in OSA
Muscle Vibration in MS to Improve Walking
What is the Nature of Pelvic Floor Muscle Involvement in Dyspareunia?
The Role of a Device to Evaluate the Neuromuscular Function in Assessing Muscle in Facial Paralysis …
Effect of Exercise Training on Protein Expression in Skeletal Muscle Tissue After Exercise in Periph…
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