Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Meckel syndrome type 8 is an autosomal recessive disorder caused by mutations in the TCTN2 gene.
Meckel syndrome
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Meckel syndrome 02
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Meckel syndrome 03
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Meckel syndrome 05
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Meckel syndrome 06
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Meckel syndrome 08
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TCTN2
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Meckel syndrome 09
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Meckel syndrome 10
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Meckel syndrome 11
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Meckel syndrome 13
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| 1. |
Shaheen R et al. (2011) A TCTN2 mutation defines a novel Meckel Gruber syndrome locus. 
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| 2. |
OMIM.ORG article Omim 613885
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