Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome-Reference-Cited by-同舟云学术

Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome

Published:2019-06 Issue:6 Volume:104 Page:1139-1157
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bauer Christiane K.,Schneeberger Pauline E.,Kortüm Fanny,Altmüller Janine,Santos-Simarro Fernando,Baker Laura,Keller-Ramey Jennifer,White Susan M.,Campeau Philippe M.,Gripp Karen W.,Kutsche Kerstin

Funder

Deutsche Forschungsgemeinschaft

Federal Ministry of Education and Research

Canadian Institutes of Health Research

Fonds de Recherche du Québec en Santé

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference80 articles.

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4. Ueber Anomalien des Ektoderms;Zimmermann;Vierteljahresschrift Zahnheilkunde.,1928

5. Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome;Kortüm;Nat. Genet.,2015

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