Extending the clinical phenotype associated with biallelic
<i>NTHL1</i>
germline mutations

Extending the clinical phenotype associated with biallelic NTHL1 germline mutations

Fostira, Florentia; Kontopodis, Emmanouil; Apostolou, Paraskevi; Fragkaki, Maria; Androulakis, Nikolaos; Yannoukakos, Drakoulis; Konstantopoulou, Irene; Saloustros, Emmanouil

期刊名称Clinical Genetics
作者Fostira, Florentia; Kontopodis, Emmanouil; Apostolou, Paraskevi; Fragkaki, Maria; Androulakis, Nikolaos; Yannoukakos, Drakoulis; Konstantopoulou, Irene; Saloustros, Emmanouil
印刷ISSN0009-9163
文件大小661.19KB
发表时间2018-09-24
DOI10.1111/cge.13444

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Extending the clinical phenotype associated with biallelic NTHL1 germline mutations