The corrected breakpoint sequence of the homozygous SPINK1 deletion causing severe infantile isolated exocrine pancreatic insufficiency - Vigipallia

0 avis

The corrected breakpoint sequence of the homozygous SPINK1 deletion causing severe infantile isolated exocrine pancreatic insufficiency

Archive ouverte

Masson, Emmanuelle | Férec, Claude | Chen, Jian-Min

Edité par CCSD ; Wiley -

International audience

Langue: en

Consulter en ligne

Consulter le document

Suggestions

Du même auteur

The three common polymorphisms p.A986S, p.R990G and p.Q1011E in the calcium sensing receptor (CASR) are not associated with chronic pancreatitis

Archive ouverte | Ewers, Maren | CCSD

International audience

Digging deeper into the intronic sequences of the SPINK1 gene

Archive ouverte | Zou, Wen-Bin | CCSD

International audience

Trypsinogen (PRSS1 and PRSS2) gene dosage correlates with pancreatitis risk across genetic and transgenic studies: a systematic review and re-analysis

Archive ouverte | Zou, Wen-Bin | CCSD

International audience

Chargement des enrichissements...