No. Panggil : | Human Molecular Genetics: Volume 22, Issue 10: 15 May 2013: p. 2055-2066 |
Judul : | Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures |
Pengarang : | |
Penerbit dan Distribusi : | United Kingdom : Oxford University Press, 2013 |
Subjek : | |
Jenis Bahan : | {007/00} |
Lokasi : |
Nomor Panggil | No. Barkod | Ketersediaan |
---|---|---|
Human Molecular Genetics: Volume 22, Issue 10: 15 May 2013: p. 2055-2066 | Human Molecular Genetics: Volume 22, Issue 10: 15 May 2013: p. 2055-2066 | TERSEDIA |
Ulasan Anggota: |
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