All individuals with variants in gene MYOCD

2 entries on 1 page. Showing entries 1 - 2.
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00225707 25558065-Fam13DG1549 PubMed: Alazami 2015, Journal: Alazami 2015 4-generation family, 2 affected sisters, unaffected heterozygous carrier parents/relatives F yes Saudi Arabia - - - - - ? see paper; …, intellectual disability and epilepsy 1 2 Johan den Dunnen
00316084 K107 PubMed: Heidet 2017 - - - France - - - - - CAKUT renal hypoplasia; preauricular pits 2 1 Johan den Dunnen
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