Concepedia

Publication | Open Access

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

DOIFull Paper Access

27

Citations

25

References

2021

Year

Felix Marbach, Georgi Stoyanov, Florian Erger, Constantine A. Stratakis, Nikolaos Settas, Edra London, Jill A. Rosenfeld, Erin Torti, Chad Haldeman‐Englert, Evgenia Sklirou,
Genetics in Medicine

References

YearCitations

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