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1 Ergebnisse
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Novel heterozygous deletion mutation c.821delC in the AAA d..:
Shigematsu, Yukiko
;
Hayashi, Ryota
;
Yoshida, Kazue
...
The Journal of Dermatology. 44 (2017) 6 - p. , 2017
Link:
https://doi.org/10.1111/1346-8138.13736
RT Journal T1
Novel heterozygous deletion mutation c.821delC in the AAA domain of BCS1L underlies Björnstad syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_1346-8138.13736&Exemplar=1&LAN=DE A1 Shigematsu, Yukiko A1 Hayashi, Ryota A1 Yoshida, Kazue A1 Shimizu, Ai A1 Kubota, Masaya A1 Komori, Manabu A1 Shimomura, Yutaka A1 Niizeki, Hironori PB Wiley YR 2017 SN 0385-2407 SN 1346-8138 JF The Journal of Dermatology VO 44 IS 6 LK http://dx.doi.org/https://doi.org/10.1111/1346-8138.13736 DO https://doi.org/10.1111/1346-8138.13736 SF ELIB - SuUB Bremen
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