Hyperchlorhidrosis Caused by Homozygous Mutation in CA12, Encoding Carbonic Anhydrase XII-Reference-Cited by-同舟云学术

Hyperchlorhidrosis Caused by Homozygous Mutation in CA12, Encoding Carbonic Anhydrase XII

Published:2010-11 Issue:5 Volume:87 Page:713-720
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Feldshtein Maya,Elkrinawi Suliman,Yerushalmi Baruch,Marcus Barak,Vullo Daniela,Romi Hila,Ofir Rivka,Landau Daniel,Sivan Sara,Supuran Claudiu T.,Birk Ohad S.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference22 articles.

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4. Nasal potential difference in non-classic cystic fibrosis-long term follow up;Jaron;Pediatr. Pulmonol.,2008

5. Lethal congenital contractural syndrome type 2 (LCCS2) is caused by a mutation in ERBB3 (Her3), a modulator of the phosphatidylinositol-3-kinase/Akt pathway;Narkis;Am. J. Hum. Genet.,2007

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