All individuals with variants in gene MCRS1

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AscendingIndividual ID     

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00065240 26942288 F3 BAB6896 PubMed: Harel 2016, Journal: Harel 2016 2-generation family, 2 affected brotherss, unaffected heterozygous carrier parents M yes Saudi Arabia - >10y - - - DD Global developmental delay (HP:0001263), Delayed speech and language development (HP:0000750), no seizures (-HP:0001250), no scoliosis (-HP:0002650), no microcephaly (Z score 0) (-HP:0000252), Deeply set eye (HP:0000490), retrognathia (HP:0000278), Muscular hypotonia of the trunk (HP:0008936), no limb hypertonia (-HP:0002509), no dystonic posturing (-HP:0002533), esotropia (HP:0000565), Hypermetropia (HP:0000540), Astigmatism (HP:0000483), Cerebellar atrophy (HP:0001272), no cerebral atrophy (-HP:0002059), Corpus callosum atrophy (HP:0007371) 1 2 Pieter Klap
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