Concepedia

Publication | Open Access

De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies

DOIFull Paper Access

21

Citations

14

References

2018

Year

Kohei Hamanaka, Yuji Sugawara, Takeyoshi Shimoji, Tone Irene Nordtveit, Mitsuhiro Kato, Mitsuko Nakashima, Hirotomo Saitsu, Toshimitsu Suzuki, Kazuhiro Yamakawa, Ingvild Aukrust,
European Journal of Human Genetics

References

YearCitations

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