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1041.
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Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects. [electronic resource] by
- Simon, Amos J
- Lev, Atar
- Zhang, Yong
- Weiss, Batia
- Rylova, Anna
- Eyal, Eran
- Kol, Nitzan
- Barel, Ortal
- Cesarkas, Keren
- Soudack, Michalle
- Greenberg-Kushnir, Noa
- Rhodes, Michele
- Wiest, David L
- Schiby, Ginette
- Barshack, Iris
- Katz, Shulamit
- Pras, Elon
- Poran, Hana
- Reznik-Wolf, Haike
- Ribakovsky, Elena
- Simon, Carlos
- Hazou, Wadi
- Sidi, Yechezkel
- Lahad, Avishay
- Katzir, Hagar
- Sagie, Shira
- Aqeilan, Haifa A
- Glousker, Galina
- Amariglio, Ninette
- Tzfati, Yehuda
- Selig, Sara
- Rechavi, Gideon
- Somech, Raz
Producer: 20170727
In:
The Journal of experimental medicine vol. 213
Availability: No items available.
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