Publication:

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Date

Date

Date
2017
Journal Article
Published version

Citations

Citation copied

Shaw, N. D., Brand, H., Kupchinsky, Z. A., Bengani, H., Plummer, L., Jones, T. I., Erdin, S., Williamson, K. A., Rainger, J., Stortchevoi, A., Samocha, K., Currall, B. B., Dunican, D. S., Collins, R. L., Willer, J. R., Lek, A., Lek, M., Nassan, M., Pereira, S., … et al. (2017). Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nature Genetics, 49, 969. https://doi.org/10.1038/ng0617-969c

Metrics

Views

134 since deposited on 2017-11-13
133last week
Acq. date: 2025-11-14

Additional indexing

Creators (Authors)

  • Shaw, Natalie D
  • Brand, Harrison
  • Kupchinsky, Zachary A
  • Bengani, Hemant
  • Plummer, Lacey
  • Jones, Takako I
  • Erdin, Serkan
  • Williamson, Kathleen A
  • Rainger, Joe
  • Stortchevoi, Alexei
  • Samocha, Kaitlin
  • Currall, Benjamin B
  • Dunican, Donncha S
  • Collins, Ryan L
  • Willer, Jason R
  • Lek, Angela
  • Lek, Monkol
  • Nassan, Malik
  • Pereira, Shahrin
  • Kammin, Tammy
  • Lucente, Diane
  • Silva, Alexandra
  • Seabra, Catarina M
  • Chiang, Colby
  • An, Yu
  • Ansari, Morad
  • Rainger, Jacqueline K
  • Joss, Shelagh
  • Smith, Jill Clayton
  • Lippincott, Margaret F
  • et al

Journal/Series Title

Journal/Series Title

Journal/Series Title

Volume

Volume

Volume
49

Number

Number

Number
6

Page range/Item number

Page range/Item number

Page range/Item number
969

Item Type

Item Type

Item Type
Journal Article

Dewey Decimal Classifikation

Dewey Decimal Classifikation

Dewey Decimal Classifikation

Language

Language

Language
English

Publication date

Publication date

Publication date
2017-05-26

Date available

Date available

Date available
2017-11-13

Publisher

Publisher

Publisher

ISSN or e-ISSN

ISSN or e-ISSN

ISSN or e-ISSN
1061-4036

OA Status

OA Status

OA Status
Closed

PubMed ID

PubMed ID

PubMed ID

Metrics

Views

134 since deposited on 2017-11-13
133last week
Acq. date: 2025-11-14

Citations

Citation copied

Shaw, N. D., Brand, H., Kupchinsky, Z. A., Bengani, H., Plummer, L., Jones, T. I., Erdin, S., Williamson, K. A., Rainger, J., Stortchevoi, A., Samocha, K., Currall, B. B., Dunican, D. S., Collins, R. L., Willer, J. R., Lek, A., Lek, M., Nassan, M., Pereira, S., … et al. (2017). Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nature Genetics, 49, 969. https://doi.org/10.1038/ng0617-969c

Closed
Loading...
Thumbnail Image

Files

Files

Files
Files available to download:1

Files

Files

Files
Files available to download:1
Loading...
Thumbnail Image