Výsledky vyhledávání - "Margot Comel"

First report of a short in‐frame biallelic deletion removing part of the EGF‐like domain calcium‐binding motif in LTBP4 and causing autosomal recessive cutis laxa type 1C

Autor: Jean‐Marie Ravel, Margot Comel, Marion Wandzel, Myriam Bronner, Aurélie Tatopoulos, Mathilde Renaud, Laëtitia Lambert, Anne‐Claire Bursztejn, Céline Bonnet

Publikováno v: American Journal of Medical Genetics Part A. 188:3343-3349

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dc70a443b2109dbf2edea2fa827bba21
https://doi.org/10.1002/ajmg.a.62954

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