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#617393 - NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION; NECFM
Cytogenetic locations: Transfer
Gene summaries Genetic tests Medical literature
*610672 - NUCLEUS ACCUMBENS-ASSOCIATED PROTEIN 1, BEN AND BTB/POZ DOMAINS-CONTAINING; NACC1
#607641 - NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 14; HMND14
Cytogenetic locations: 2p13.2
*601143 - DYNACTIN 1; DCTN1
#168605 - PERRY SYNDROME
#105400 - AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE, INCLUDED
Cytogenetic locations: 1p36, 1p36, 1p36, 1p36
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