Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations - Concepedia

Concepedia

Publication | Open Access

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

DOI Full Paper Access

490

Citations

18

References

2010

Year

Kaya Bilgüvar, Ali K. Ozturk, Angeliki Louvi, Kenneth Y. Kwan, Murim Choi, Dilek Yalnızoğlu, Beyhan Tüysüz, Ahmet Okay Çağlayan, Sarenur Gökben, Hande Kaymakçalan,

Mendelian DisorderGenetic DisorderGeneticsSevere Brain MalformationsNeurologyNeuroscienceDisease Gene IdentificationBrain PathologyNeuropathologyMedicineNeurogenetics

References

	Year	Citations

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