homozygous FANCM mutationn underlies a familial case of non-syndromic primary ovarian insufficiency

Rousselle Tr Théo; Roxanne Hablot

Journal Articles eLife Year : 2022

homozygous FANCM mutationn underlies a familial case of non-syndromic primary ovarian insufficiency

(1) ,

1

Rousselle Tr Théo

Function : Author
PersonId : 1198745

Unité de Biologie Fonctionnelle et Adaptative

Roxanne Hablot

Function : Author
PersonId : 749844
IdHAL : roxanne-hablot

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Life Sciences [q-bio] Animal biology

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elife-30490-v2.pdf (1.79 Mo)

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Théo Rousselle : Connect in order to contact the contributor

https://hal-cnrs.archives-ouvertes.fr/hal-03886811

Submitted on : Tuesday, December 6, 2022-2:42:46 PM

Last modification on : Wednesday, December 14, 2022-3:33:01 PM

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hal-03886811 , version 1 (06-12-2022)

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HAL Id : hal-03886811 , version 1

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Rousselle Tr Théo, Roxanne Hablot. homozygous FANCM mutationn underlies a familial case of non-syndromic primary ovarian insufficiency. eLife, 2022. ⟨hal-03886811⟩

homozygous FANCM mutationn underlies a familial case of non-syndromic primary ovarian insufficiency

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