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C14orf119 gene
Known as:
C14orf119
, FLJ20671
, chromosome 14 open reading frame 119
National Institutes of Health
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1 relation
Chromosomes, Human, Pair 14
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2020
2020
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders
Toshimitsu Suzuki
,
Toshifumi Suzuki
,
+26 authors
K. Yamakawa
Annals of Clinical and Translational Neurology
2020
Corpus ID: 219606055
Neurodevelopmental disorders (NDDs) often associate with epilepsy or craniofacial malformations. Recent large‐scale DNA analyses…
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