All individuals with variants in gene DSCAML1

6 entries on 1 page. Showing entries 1 - 6.
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00150202 26539891-FamBAB5192 PubMed: Karaca 2015 - - - - - - - family structure in paper - ? Motor neuron disease, scoliosis, chest deformity (secondary to motor neuron disease?) 1 1 Johan den Dunnen
00326435 AVM285 PubMed: Wang 2018 - - - China - - - - - ? - 2 1 Johan den Dunnen
00326444 AVM106 PubMed: Wang 2018 - - - China - - - - - ? - 2 1 Johan den Dunnen
00332249 FamB PubMed: Astuti 2018 2-generation family, 1 affected, unaffected parents - - Netherlands - - - - - retinal disease see paper; ... 1 1 LOVD
00377956 - PubMed: _Audo-2012 false positive, not found by Sanger - - - - - - - - retinal disease - 1 1 LOVD
00401208 family PubMed: Naqvi 2022 5-generation family, 7 affected (4F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - MCPH see paper; ..., small heads, mild-moderate intellectual disability, short stature, narrow and oval shaped faces, receding foreheads, large ears, prominent nose; attention deficit behavior, speech apraxia; never attended school; affected males spend time wandering streets, no concept of money, not able to perform any conceptual work, recognize relatives, find their way home, sense of self-respect, comfortable with strangers and are friendly 1 1 Johan den Dunnen
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