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Meckel syndrome 08

Meckel syndrome type 8 is an autosomal recessive disorder caused by mutations in the TCTN2 gene.

Systematic

Meckel syndrome
Meckel syndrome 02
Meckel syndrome 03
Meckel syndrome 05
Meckel syndrome 06
Meckel syndrome 08
TCTN2
Meckel syndrome 09
Meckel syndrome 10
Meckel syndrome 11
Meckel syndrome 13

References:

1.

Shaheen R et al. (2011) A TCTN2 mutation defines a novel Meckel Gruber syndrome locus.

external link
2.

OMIM.ORG article

Omim 613885 external link
Update: Aug. 14, 2020
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