Results
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69241.
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69242.
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69243.
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69244.
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69252.
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69253.
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69254.
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69255.
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Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder. [electronic resource] by
- Kumar, Raman
- Corbett, Mark A
- Smith, Nicholas J C
- Jolly, Lachlan A
- Tan, Chuan
- Keating, Damien J
- Duffield, Michael D
- Utsumi, Toshihiko
- Moriya, Koko
- Smith, Katherine R
- Hoischen, Alexander
- Abbott, Kim
- Harbord, Michael G
- Compton, Alison G
- Woenig, Joshua A
- Arts, Peer
- Kwint, Michael
- Wieskamp, Nienke
- Gijsen, Sabine
- Veltman, Joris A
- Bahlo, Melanie
- Gleeson, Joseph G
- Haan, Eric
- Gecz, Jozef
Producer: 20160113
In:
Human molecular genetics vol. 24
Availability: No items available.
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69256.
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