Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations - Concepedia

Concepedia

Publication | Open Access

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

DOI Full Paper Access

124

Citations

36

References

2013

Year

Claudio Toma, Bàrbara Torrico, Amaia Hervás, Rafael Valdés‐Mas, Alba Tristán‐Noguero, Vanesa Padillo, Marta Maristany, Marta Morgade Salgado, C. Arenas, Xosé S. Puente,

Molecular Psychiatry

Heterozygous Truncating MutationsMendelian DisorderSyndromic AutismExome SequencingGeneticsGenetic DisorderFragile X SpectrumMolecular BiologyAutismMolecular GeneticsDisease Gene IdentificationGenomicsMedicineMultiplex Autism Families

References

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