WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study (Englisch)
- Neue Suche nach: Yuan, J.‐H.
- Neue Suche nach: Hashiguchi, A.
- Neue Suche nach: Yoshimura, A.
- Neue Suche nach: Sakai, N.
- Neue Suche nach: Takahashi, M.P.
- Neue Suche nach: Ueda, T.
- Neue Suche nach: Taniguchi, A.
- Neue Suche nach: Okamoto, S.
- Neue Suche nach: Kanazawa, N.
- Neue Suche nach: Yamamoto, Y.
- Neue Suche nach: Saigoh, K.
- Neue Suche nach: Kusunoki, S.
- Neue Suche nach: Ando, M.
- Neue Suche nach: Hiramatsu, Y.
- Neue Suche nach: Okamoto, Y.
- Neue Suche nach: Takashima, H.
- Neue Suche nach: Yuan, J.‐H.
- Neue Suche nach: Hashiguchi, A.
- Neue Suche nach: Yoshimura, A.
- Neue Suche nach: Sakai, N.
- Neue Suche nach: Takahashi, M.P.
- Neue Suche nach: Ueda, T.
- Neue Suche nach: Taniguchi, A.
- Neue Suche nach: Okamoto, S.
- Neue Suche nach: Kanazawa, N.
- Neue Suche nach: Yamamoto, Y.
- Neue Suche nach: Saigoh, K.
- Neue Suche nach: Kusunoki, S.
- Neue Suche nach: Ando, M.
- Neue Suche nach: Hiramatsu, Y.
- Neue Suche nach: Okamoto, Y.
- Neue Suche nach: Takashima, H.
In:
Clinical Genetics
;
92
, 6
;
659-663
;
2017
- Aufsatz (Zeitschrift) / Elektronische Ressource
-
Titel:WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study
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Beteiligte:Yuan, J.‐H. ( Autor:in ) / Hashiguchi, A. ( Autor:in ) / Yoshimura, A. ( Autor:in ) / Sakai, N. ( Autor:in ) / Takahashi, M.P. ( Autor:in ) / Ueda, T. ( Autor:in ) / Taniguchi, A. ( Autor:in ) / Okamoto, S. ( Autor:in ) / Kanazawa, N. ( Autor:in ) / Yamamoto, Y. ( Autor:in )
-
Erschienen in:Clinical Genetics ; 92, 6 ; 659-663
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Verlag:
- Neue Suche nach: Blackwell Publishing Ltd
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Erscheinungsdatum:01.12.2017
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Format / Umfang:5 pages
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ISSN:
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DOI:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Elektronische Ressource
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Sprache:Englisch
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Schlagwörter:
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Datenquelle:
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